FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathy-Reference-Cited by-同舟云学术

FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathy

Published:2016-01-11 Issue:1 Volume:17 Page:
ISSN:1474-760X
Container-title:Genome Biology
language:en
Short-container-title:Genome Biol

Author:

Al-Yacoub Nadya,Shaheen Ranad,Awad Salma Mahmoud,Kunhi Muhammad,Dzimiri Nduna,Nguyen Henry C.,Xiong Yong,Al-Buraiki Jehad,Al-Habeeb Waleed,Alkuraya Fowzan S.,Poizat Coralie

Funder

King Abdulaziz City for Science and Technology

Institutional funds

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1186/s13059-015-0861-4.pdf

Reference34 articles.

1. Towbin JA. Inherited cardiomyopathies. Circ J. 2014;78:2347–56.

2. Jefferies JL, Towbin JA. Dilated cardiomyopathy. Lancet. 2010;375:752–62.

3. Schonberger J, Seidman CE. Many roads lead to a broken heart: the genetics of dilated cardiomyopathy. Am J Hum Genet. 2001;69:249–60.

4. Hershberger RE, Hedges DJ, Morales A. Dilated cardiomyopathy: the complexity of a diverse genetic architecture. Nat Rev Cardiol. 2013;10:531–47.

5. Grunig E, Tasman JA, Kucherer H, Franz W, Kubler W, Katus HA. Frequency and phenotypes of familial dilated cardiomyopathy. J Am Coll Cardiol. 1998;31:186–94.

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