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Myozenin 2 Is a Novel Gene for Human Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a genetic disorder caused by mutations in sarcomeric proteins (excluding phenocopy). The causal genes in approximately one-third of the cases remain unknown. We identified a family comprised of 6 clinically affected members. The phenotype was characterized by ear...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Osio, Adriana, Tan, Lily, Chen, Suet N., Lombardi, Raffaella, Nagueh, Sherif F., Shete, Sanjay, Roberts, Robert, Willerson, James T., Marian, Ali J.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2007
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2775141/
https://ncbi.nlm.nih.gov/pubmed/17347475
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/01.RES.0000263008.66799.aa
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