A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
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A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
description
2018 nî lūn-bûn
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2018年の論文
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2018年学术文章
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2018年学术文章
@zh-cn
2018年学术文章
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name
A novel homozygous variant of ...... by next generation sequencing.
@en
A novel homozygous variant of ...... by next generation sequencing.
@nl
type
label
A novel homozygous variant of ...... by next generation sequencing.
@en
A novel homozygous variant of ...... by next generation sequencing.
@nl
prefLabel
A novel homozygous variant of ...... by next generation sequencing.
@en
A novel homozygous variant of ...... by next generation sequencing.
@nl
P2093
P2860
P1433
P1476
A novel homozygous variant of ...... by next generation sequencing.
@en
P2093
Chunli Wei
Elaine Lai-Han Leung
Hongbin Lv
Jingliang Cheng
Lisha Yang
Saber Imani
Shangyi Fu
P2860
P2888
P356
10.1186/S12881-018-0602-0
P50
P577
2018-06-11T00:00:00Z
P6179
1104522261