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Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation

Detalles Bibliográficos
Autores principales:	Alsters, S., Wong, L., Peferoen, L., Niessen, H. W. M., Bikker, H., Elting, M. W., Houweling, A. C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bohn Stafleu van Loghum 2019
Materias:	Heart Beat
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470222/ https://www.ncbi.nlm.nih.gov/pubmed/30742251 http://dx.doi.org/10.1007/s12471-019-1245-2

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