(Q45985544)

English

Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy.

scientific article published in February 2009

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

mitochondrial DNA

0 references

nucleic acid sequence analysis

1 reference

based on heuristic

inferred from title

author name string

Iris Schrijver

1

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Lynn M Pique

2

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Ilana Traynis

3

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Curt Scharfe

4

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Amy J Sehnert

5

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

language of work or name

0 references

publication date

1 February 2009

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

11

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

2

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

118-126

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

https://scigraph.springernature.com/pub.10.1097/gim.0b013e318190356b

0 references

The Incidence of Pediatric Cardiomyopathy in Two Regions of the United States

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

The Epidemiology of Childhood Cardiomyopathy in Australia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Comparison of fluorescent SSCP and denaturing HPLC analysis with direct sequencing for mutation screening in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Clinical presentations of mitochondrial cardiomyopathies

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Cardiomyopathy in respiratory chain disorders

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Qualitative and quantitative detection of mitochondrial heteroplasmy in cerebrospinal fluid using denaturing high-performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Rapid screening mitochondrial DNA mutation by using denaturing high-performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Quantitative mitochondrial DNA mutation analysis by denaturing HPLC.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Pitfalls in the denaturing high-performance liquid chromatography analysis of mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

High incidence of pre-excitation syndrome in Japanese families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Mitochondrial deafness

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Techniques and Pitfalls in the Detection of Pathogenic Mitochondrial DNA Mutations

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Mitochondrial respiratory chain disorders I: mitochondrial DNA defects

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318190356B

21 January 2018

Identifiers

10.1097/GIM.0B013E318190356B

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19265752

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q45985544&oldid=1459930770"