Neonatal case of dilated cardiomyopathy associated with novel MYH7 and TBX5 genetic variants
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چکیده
منابع مشابه
A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy.
Dilated cardiomyopathy (DCM) represents the most prevalent form of primary cardiomyopathy, and is the most common reason for heart transplantation and a major cause of congestive heart failure. Aggregating evidence demonstrates that genetic defects are associated with DCM, and a great number of mutations in >50 genes have been linked to DCM. However, DCM is a genetically heterogeneous disorder ...
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ژورنال
عنوان ژورنال: Nauchno-prakticheskii zhurnal «Medicinskaia genetika»
سال: 2020
ISSN: 2073-7998
DOI: 10.25557/2073-7998.2020.05.16-17