Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

We identified a unique family with autosomal dominant heart disease variably expressed as restrictive cardiomyopathy (RCM), hypertrophic cardiomyopathy (HCM), and dilated cardiomyopathy (DCM), and sought to identify the molecular defect that triggered divergent remodeling pathways. Polymorphic DNA m...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Menon, SC, Michels, VV, Pellikka, PA, Ballew, JD, Karst, ML, Herron, KJ, Nelson, SM, Rodeheffer, RJ, Olson, TM
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2008
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2575134/
https://ncbi.nlm.nih.gov/pubmed/18651846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2008.01062.x
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