Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome.
about
Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh-hant
name
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@en
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@nl
type
label
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@en
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@nl
prefLabel
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@en
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@nl
P2093
P2860
P356
P1476
Two patients with the heterozy ...... h muscle dysfunction syndrome.
@en
P2093
Andreas Hahn
Axel Weber
Bernd A Neubauer
Birgit Lorenz
Christoph Friedburg
Dietmar Schranz
Hakan Akintuerk
Karoline Hofmann
Michael Graef
P2860
P304
P356
10.1002/AJMG.A.38102
P407
P577
2017-04-01T00:00:00Z