Digenic inheritance of mutations in the cardiac troponin ( TNNT2 ) and cardiac beta myosin heavy chain ( MYH7 ) as the cause of severe dilated cardiomyopathy-Reference-Cited by-同舟云学术

Digenic inheritance of mutations in the cardiac troponin ( TNNT2 ) and cardiac beta myosin heavy chain ( MYH7 ) as the cause of severe dilated cardiomyopathy

Published:2017-09 Issue:9 Volume:60 Page:485-488
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Petropoulou Evmorfia,Soltani Mohammadhossein,Firoozabadi Ali Dehghani,Namayandeh Seyedeh Mahdieh,Crockford Jade,Maroofian Reza,Jamshidi Yalda

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference17 articles.

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3. Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C;Gruen;J. Mol. Biol.,1999

4. Atlas of the clinical genetics of human dilated cardiomyopathy;Haas;Eur. Heart J.,2015

5. Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies;Hoedemaekers;Eur. Heart J.,2007

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