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Familial hypertrophic cardiomyopathy 24
- ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
- ... HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; ...
- ... Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. ...
- ... Hassan AS]. N Engl J Med 2002 Jan 24;346(4):300. Citation on PubMed Light PE. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen ...
- ... their genetic cause. The most common form of familial partial lipodystrophy ... muscle (cardiomyopathy), a form of heart disease called coronary artery ...
- ... isolated hyperCKemia, and a heart disorder called hypertrophic cardiomyopathy. ... within the same family.Some people with rippling muscle disease do not ...
- ... muscle disease, and a heart disorder called hypertrophic cardiomyopathy. Several CAV3 gene mutations have been found ... This condition is inherited in an autosomal ...
- ... isolated hyperCKemia, and a heart disorder called hypertrophic cardiomyopathy. Several CAV3 gene mutations have been ... This condition is inherited in an autosomal ...
- ... in childhood. Eur J Hum Genet. 2016 Aug;24(8):1112-6. doi: 10.1038/ejhg.2015. ... doi: 10.1093/hmg/ddt521. Epub 2013 Oct 24. Citation on PubMed Schiff M, Haberberger B, Xia ...
- ... J Hum Genet. 2015 Mar;23(3):317-24. doi: 10.1038/ejhg.2014.115. Epub 2014 ...