Hypertrophic cardiomyopathy: from mutation to functional analysis of defective protein

AIM: To analyze the genesis of hypertrophic cardiomyopathy on a large cohort of patients from molecular genetics point of view and perform the functional analysis of the 3D molecular model of defective myosin-7 protein in silico. METHODS: The study enrolled 153 patients with diagnosed hypertrophic c...

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Detalles Bibliográficos
Autores principales: Capek, Pavel, Vondrasek, Jiri, Skvor, Jiri, Brdicka, Radim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2011
Materias:
Molecular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118724/
https://www.ncbi.nlm.nih.gov/pubmed/21674835
http://dx.doi.org/10.3325/cmj.2011.52.384

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118724/
https://www.ncbi.nlm.nih.gov/pubmed/21674835
http://dx.doi.org/10.3325/cmj.2011.52.384

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