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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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-30742251
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Neth Heart J Year: 2019 Document type: Article Affiliation country: Países Bajos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Neth Heart J Year: 2019 Document type: Article Affiliation country: Países Bajos