Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2013

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اینتگرین آلفا ۷

Cited by user Tisfoon on 24 Aug 2019

ITGA7

Cited by user HeartBD2K Scruggssb on 20 Jul 2015

Integrin alpha-7 is a protein that in humans is encoded by the ITGA7 gene. Alpha-7 integrin is critical for modulating cell-matrix interactions.

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