Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death.
about
Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death.
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-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
2017年學術文章
@zh-hant
name
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@en
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@nl
type
label
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@en
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@nl
prefLabel
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@en
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@nl
P2093
P2860
P356
P1476
Homozygous EEF1A2 mutation cau ...... lay, epilepsy and early death.
@en
P2093
Brandon S Guida
Catherine A Brownstein
Elizabeth Blume
Laura L Smith
Michael C Kruer
Pankaj B Agrawal
Sarah U Morton
Sergio R Padilla-Lopez
P2860
P304
P356
10.1093/HMG/DDX239
P577
2017-09-01T00:00:00Z