Medical Xpress Severe forms of congenital heart disease caused by variants of the NR2F2 gene Medical Xpress Family charts and sequencing results of NR2F2 variants in eight families affected by congenital heart disease.
The HCMA, Hypertrophic Cardiomyopathy Association provides information, support and advocacy for those with HCM, their families and the medical community. HCM is a common genetic heart condition affecting 1 in 500 people.
The HCMA YouTube Channel provides a lot of information that makes a difference!
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