A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia-Reference-Cited by-同舟云学术

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

Published:2009-01-18 Issue:2 Volume:41 Page:187-191
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Dhandapany Perundurai S,Sadayappan Sakthivel,Xue Yali,Powell Gareth T,Rani Deepa Selvi,Nallari Prathiba,Rai Taranjit Singh,Khullar Madhu,Soares Pedro,Bahl Ajay,Tharkan Jagan Mohan,Vaideeswar Pradeep,Rathinavel Andiappan,Narasimhan Calambur,Ayapati Dharma Rakshak,Ayub Qasim,Mehdi S Qasim,Oppenheimer Stephen,Richards Martin B,Price Alkes L,Patterson Nick,Reich David,Singh Lalji,Tyler-Smith Chris,Thangaraj Kumarasamy

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.309.pdf

Reference28 articles.

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2. Joshi, P. et al. Risk factors for early myocardial infarction in South Asians compared with individuals in other countries. J. Am. Med. Assoc. 297, 286–294 (2007).

3. Liew, C.C. & Dzau., V. J. Molecular genetics and genomics of heart failure. Nat. Rev. Genet. 5, 811–825 (2004).

4. Flavigny, J. et al. Biomolecular interactions between human recombinant h-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy. Cardiovasc. Res. 60, 388–396 (2003).

5. Flavigny, J. et al. COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes. J. Mol. Biol. 294, 443–456 (1999).

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