(Q34288212)

1 August 2017

title

New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies (English)

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1 August 2017

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Tiina Ojala

1

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1 August 2017

Padmini Polinati

2

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1 August 2017

Tuula Manninen

3

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1 August 2017

Anita Hiippala

4

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1 August 2017

Jukka Rajantie

5

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1 August 2017

Riitta Karikoski

6

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1 August 2017

Anu Suomalainen

7

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1 August 2017

Tiina Tyni

8

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1 August 2017

language of work or name

English

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publication date

13 July 2012

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1 August 2017

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1 August 2017

volume

72

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1 August 2017

issue

4

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1 August 2017

page(s)

432-437

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Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

The 3‐methylglutaconic acidurias: what's new?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Tafazzin knockdown causes hypertrophy of neonatal ventricular myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

The HSP70 chaperone machinery: J proteins as drivers of functional specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Isolated ventricular non-compaction of the myocardium in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Echocardiographic diagnosis and prognosis of fetal left ventricular noncompaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Gene mutations in apical hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Permanent cardiac pacing in a 2.5 month-old infant with severe cyanotic breath-holding spells and prolonged asystole

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.92

31 March 2020

Identifiers

DOI

10.1038/PR.2012.92

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Dimensions Publication ID

1 August 2017

1010948096

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1 reference