Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation.

Alsters, S; Wong, L; Peferoen, L; Niessen, H W M; Bikker, H; Elting, M W; Houweling, A C

Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation.

Alsters, S; Wong, L; Peferoen, L; Niessen, H W M; Bikker, H; Elting, M W; Houweling, A C.

Afiliación

Alsters S; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Wong L; Department of Cardiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Peferoen L; Department of Pathology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Niessen HWM; Department of Pathology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Bikker H; Department of Clinical Genetics, Amsterdam UMC, Academic Medical Center, Amsterdam, The Netherlands.
Elting MW; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Houweling AC; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. a.houweling@vumc.nl.

Neth Heart J ; 27(5): 282-283, 2019 May.

Article en En | MEDLINE | ID: mdl-30742251

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neth Heart J Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Países Bajos

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