(Q34469735)

2 August 2017

1 reference

title

Molecular genetic basis of sudden cardiac death. (English)

1 reference

2 August 2017

Towbin JA

1

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2 August 2017

1 November 2001

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2 August 2017

Cardiovascular Pathology

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2 August 2017

10

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2 August 2017

6

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2 August 2017

283-295

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Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Low penetrance in the long-QT syndrome: clinical impact

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial Q-T prolongation syndrome. Convulsive seizures and paroxysmal ventricular fibrillation.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

QT-Interval Prolongation, Paroxysmal Ventricular Arrhythmias, and Convulsive Syncope

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Prolonged QT period in diabetic autonomic neuropathy: a possible role in sudden cardiac death?

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Autonomic neuropathy, QT interval lengthening, and unexpected deaths in male diabetic patients

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

The congenital long QT syndromes in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Long QT syndrome associated with syndactyly identified in females

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Cardiac Innervation, Neonatal Electrocardiography, and SIDS

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Prolongation of the QT interval and the sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Prolongation of the QT interval and the sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Congenital deafness and cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A recessive variant of the Romano-Ward long-QT syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

New mutations in the KVLQT1 potassium channel that cause long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A family of potassium channel genes related to eag in Drosophila and mammals

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

HERG- and IRK-like inward rectifier currents are sequentially expressed during neuronal development of neural crest cells and their derivatives.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Idiosyncratic gating of HERG-like K+ channels in microglia

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

1 reference

7 January 2021

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

HERG, a human inward rectifier in the voltage-gated potassium channel family

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A minK-HERG complex regulates the cardiac potassium current I(Kr)

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Selective localization of cardiac SCN5A sodium channels in limbic regions of rat brain.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Molecular basis of the long-QT syndrome associated with deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Elevation of the RS-T segment, apparent or real, in the right precordial leads as a probable normal variant

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Dialyzable currents of injury in potassium intoxication resembling acute myocardial infarction or pericarditis

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Ventricular fibrillation without apparent heart disease: description of six cases

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A HISTOPATHOLOGICAL STUDY ON THE CONDUCTION SYSTEM OF THE SO-CALLED "POKKURI DISEASE" : SUDDENUNEXPECTED CARDIAC DEATH OF UNKNOWN ORIGIN IN JAPAN

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Sudden nocturnal death in young males from ventricular flutter

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Further characterization of the syndrome of right bundle branch block, ST segment elevation, and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial occurrence of electrocardiographic abnormalities of the Brugada-type

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

The Brugada syndrome: clinical, electrophysiologic and genetic aspects.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

1 reference

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Differences in the electrophysiological response of canine ventricular epicardium and endocardium to ischemia. Role of the transient outward current

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Differences in the electrophysiological response of canine ventricular subendocardium and subepicardium to acetylcholine and isoproterenol. A direct effect of acetylcholine in ventricular myocardium

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Ion channels and ventricular arrhythmias: cellular and ionic mechanisms underlying the Brugada syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Flecainide-induced arrhythmia in canine ventricular epicardium. Phase 2 reentry?

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Sodium channel block produces opposite electrophysiological effects in canine ventricular epicardium and endocardium.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Brugada syndrome and sudden cardiac death in children

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy a still underrecognized clinic entity

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Right ventricular cardiomyopathy and sudden death in young people

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International S

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial cardiomyopathy associated with right bundle branch block, ST segment elevation and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Is the Brugada syndrome a distinct clinical entity?

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Idiopathic ventricular fibrillation of the Brugada type: an atypical form of arrhythmogenic right ventricular cardiomyopathy?

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Hypertrophic cardiomyopathy. The importance of the site and the extent of hypertrophy. A review

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Familial hypertrophic cardiomyopathy: from mutations to functional defects

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Molecular diversity of myofibrillar proteins: gene regulation and functional significance

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Alterations in Ca2+ sensitive tension due to partial extraction of C-protein from rat skinned cardiac myocytes and rabbit skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human development

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Isoform Transitions of the Myosin Binding Protein C Family in Developing Human and Mouse Muscles

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

The molecular basis for tropomyosin isoform diversity

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Human cardiac troponin T: cloning and expression of new isoforms in the normal and failing heart

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Molecular cloning of human cardiac troponin T isoforms: expression in developing and failing heart.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Troponin I isoform expression in human heart

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Sudden death due to troponin T mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

Angiotensin-converting enzyme gene polymorphism in Japanese patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

The role of cytoskeletal proteins in cardiomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS1054-8807%2801%2900090-4

7 January 2021

10.1016/S1054-8807(01)00090-4

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

11755374