Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members-Reference-Cited by-同舟云学术

Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members

Published:2017-02-17 Issue:3 Volume:173 Page:699-705
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Rafiq Muhammad Arshad¹²,Chaudhry Ayeshah³,Care Melanie⁴,Spears Danna A.⁵,Morel Chantal F.⁴,Hamilton Robert M.¹

Affiliation:

1. Physiology and Experimental Medicine; The Hospital for Sick Children and Research Institute; Toronto Ontario Canada

2. Department of Bio-Sciences; COMSATS Institute of Information Technology (CIIT); Islamabad Pakistan

3. Division of Clinical and Metabolic Genetics; The Hospital for Sick Children; University of Toronto; Toronto Ontario Canada

4. Fred A. Litwin Family Center in Genetic Medicine; University Health Network; University of Toronto; Toronto Ontario Canada

5. Division of Cardiology; University Health Network; University of Toronto; Toronto Ontario Canada

Funder

Rare Disease Foundation and BC Children's Hospital Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference28 articles.

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3. Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations;Arimura;Cardiovasc Res,2013

4. Partial left ventriculectomy-the Batista procedure;Batista;Eur J Cardiothorac Surg,1999

5. Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians;Chami;Can J Cardiol,2014

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