Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.
about
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.
description
2018 nî lūn-bûn
@nan
2018年の論文
@ja
2018年学术文章
@wuu
2018年学术文章
@zh
2018年学术文章
@zh-cn
2018年学术文章
@zh-hans
2018年学术文章
@zh-my
2018年学术文章
@zh-sg
2018年學術文章
@yue
2018年學術文章
@zh-hant
name
Compound heterozygous loss-of- ...... ardiomyopathy in two siblings.
@en
Compound heterozygous loss-of- ...... ardiomyopathy in two siblings.
@nl
type
label
Compound heterozygous loss-of- ...... ardiomyopathy in two siblings.
@en
Compound heterozygous loss-of- ...... ardiomyopathy in two siblings.
@nl
prefLabel
Compound heterozygous loss-of- ...... ardiomyopathy in two siblings.
@en
Compound heterozygous loss-of- ...... ardiomyopathy in two siblings.
@nl
P2093
P2860
P50
P1433
P1476
Compound heterozygous loss-of- ...... cardiomyopathy in two siblings
@en
P2093
Anniek Corveleyn
Céline Verdood
Jeroen Breckpot
Marc Gewillig
Xiaowen Chen
Yaojuan Jia
P2860
P304
P356
10.1371/JOURNAL.PGEN.1007138
P577
2018-01-22T00:00:00Z