(Q46904563)

26 December 2017

title

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity (English)

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26 December 2017

left ventricular noncompaction

main subject

patient

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20

Jeffrey A Towbin

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26 December 2017

author name string

Yanlin Xing

1

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26 December 2017

Fukiko Ichida

2

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26 December 2017

Taro Matsuoka

3

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26 December 2017

Takeshi Isobe

4

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26 December 2017

Yumiko Ikemoto

5

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26 December 2017

Takashi Higaki

6

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26 December 2017

Tohru Tsuji

7

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26 December 2017

Noriyuki Haneda

8

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26 December 2017

Atsushi Kuwabara

9

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26 December 2017

Rui Chen

10

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26 December 2017

Takeshi Futatani

11

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26 December 2017

Shinichi Tsubata

12

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26 December 2017

Sayaka Watanabe

13

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26 December 2017

Kazuhiro Watanabe

14

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26 December 2017

Keiichi Hirono

15

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26 December 2017

Keiichiro Uese

16

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26 December 2017

Toshio Miyawaki

17

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26 December 2017

Karla R Bowles

18

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26 December 2017

Neil E Bowles

19

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26 December 2017

publication date

19 January 2006

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26 December 2017

Molecular Genetics and Metabolism

published in

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26 December 2017

volume

88

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26 December 2017

page(s)

71-77

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26 December 2017

issue

1

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26 December 2017

Isolated noncompaction of left ventricular myocardium. A study of eight cases

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1 reference

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7 January 2021

1 reference

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Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

7 January 2021

1 reference

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Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.009

Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.009

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.11.009

A novel X-linked gene, G4.5. is responsible for Barth syndrome

7 January 2021

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

7 January 2021

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The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

7 January 2021

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An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

7 January 2021

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The genomic organization of human dystrobrevin

7 January 2021

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The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives

7 January 2021

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ZASP: a new Z-band alternatively spliced PDZ-motif protein

7 January 2021

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Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy

7 January 2021

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7 January 2021

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Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy

7 January 2021

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A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

7 January 2021

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Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients

7 January 2021

1 reference

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Genetic heterogeneity of isolated noncompaction of the left ventricular myocardium

7 January 2021

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Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis

7 January 2021

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Isolated left ventricular noncompaction: an unclassified cardiomyopathy with severe prognosis in adults

7 January 2021

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Molecular genetics of left ventricular dysfunction

7 January 2021

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Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

7 January 2021

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Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children

7 January 2021

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Fabry disease: focus on cardiac manifestations and molecular mechanisms.

7 January 2021

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Mutations in ZASP define a novel form of muscular dystrophy in humans

7 January 2021

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10.1016/J.YMGME.2005.11.009

7 January 2021

Identifiers

DOI

1 reference

26 December 2017

PubMed ID

16427346

1 reference

26 December 2017