Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase-Reference-Cited by-同舟云学术

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Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase

Published:2010-06-16 Issue:10 Volume:18 Page:1160-1165
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Levitas Aviva,Muhammad Emad,Harel Gali,Saada Ann,Caspi Vered Chalifa,Manor Esther,Beck John C,Sheffield Val,Parvari Ruti

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201083.pdf

Reference35 articles.

1. Towbin JA, Lowe AM, Colan SD et al: Incidence, causes, and outcomes of dilated cardiomyopathy in children. JAMA 2006; 296: 1867–1876.

2. Kärkkäinen S, Peuhkurinen K : Genetics of dilated cardiomyopathy. Ann Med 2007; 39: 91–107.

3. Di Donato S : Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegeneration. J Inherit Metab Dis 2000; 23: 247–263.

4. Ibdah JA, Bennett MJ, Rinaldo P et al: A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women. N Engl J Med 1999; 340: 1723–1731.

5. Spiekerkoetter U, Eeds A, Yue Z, Haines J, Strauss AW, Summar M : Uniparental disomy of chromosome 2 resulting in lethal trifunctional protein deficiency due to homozygous alpha-subunit mutations. Hum Mutat 2002; 20: 447–451.

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