A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy-Reference-Cited by-同舟云学术

A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

Published:2016-01-14 Issue:1 Volume:17 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Al-Hassnan Zuhair N.,Shinwari Zarghuna MA.,Wakil Salma M.,Tulbah Sahar,Mohammed Shamayel,Rahbeeni Zuhair,Alghamdi Mohammed,Rababh Monther,Colak Dilek,Kaya Namik,Al-Fayyadh Majid,Alburaiki Jehad

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-016-0267-5.pdf

Reference26 articles.

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2. Boucek MM, Aurora P, Edwards LB, Taylor DO, Trulock EP, Christie J, et al. Registry of the International Society for Heart and Lung Transplantation: tenth official pediatric heart transplantation report--2007. J Heart LungTransplant. 2007;26:796–807.

3. Hershberger RE, Morales A, Siegfried JD. Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals. Genet Med. 2010;12:655–67.

4. Online Mendelian Inheritance in Man. http://omim.org . (accessed 22 June 2014).

5. Willis MS, Townley-Tilson WH, Kang EY, Homeister JW, Patterson C. Sent to destroy: the ubiquitin proteasome system regulates cell signaling and protein quality control in cardiovascular development and disease. Circ Res. 2010;106(3):463–78.

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