Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation
Neth Heart J
.
2019 May;27(5):282-283.
doi: 10.1007/s12471-019-1245-2.
Authors
S Alsters
1
,
L Wong
2
,
L Peferoen
3
,
H W M Niessen
3
,
H Bikker
4
,
M W Elting
1
,
A C Houweling
5
Affiliations
1
Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
2
Department of Cardiology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
3
Department of Pathology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
4
Department of Clinical Genetics, Amsterdam UMC, Academic Medical Center, Amsterdam, The Netherlands.
5
Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. a.houweling@vumc.nl.
PMID:
30742251
PMCID:
PMC6470222
DOI:
10.1007/s12471-019-1245-2
No abstract available