A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
about
A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
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-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
2018年學術文章
@zh-hant
name
A case report: a heterozygous ...... yopathies in a Chinese family.
@en
A case report: a heterozygous deletion
@nl
type
label
A case report: a heterozygous ...... yopathies in a Chinese family.
@en
A case report: a heterozygous deletion
@nl
prefLabel
A case report: a heterozygous ...... yopathies in a Chinese family.
@en
A case report: a heterozygous deletion
@nl
P2093
P2860
P1433
P1476
A case report: a heterozygous ...... yopathies in a Chinese family.
@en
P2093
Fei-Fei Su
Xiao-Jing Wei
Xue-Fan Yu
Xue-Mei Liu
P2860
P2888
P356
10.1186/S12883-018-1078-4
P577
2018-06-04T00:00:00Z
P6179
1104385384