Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family.
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Exome sequencing identifies a novel frameshift mutation of MYO6 as the cause of autosomal dominant nonsyndromic hearing loss in a Chinese family.
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2014 nî lūn-bûn
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2014年の論文
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@yue
2014年論文
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2014年論文
@zh-hk
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Exome sequencing identifies a ...... ring loss in a Chinese family.
@en
Exome sequencing identifies a ...... ring loss in a Chinese family.
@nl
type
label
Exome sequencing identifies a ...... ring loss in a Chinese family.
@en
Exome sequencing identifies a ...... ring loss in a Chinese family.
@nl
prefLabel
Exome sequencing identifies a ...... ring loss in a Chinese family.
@en
Exome sequencing identifies a ...... ring loss in a Chinese family.
@nl
P2093
P2860
P356
P1476
Exome sequencing identifies a ...... ring loss in a Chinese family.
@en
P2093
Dongyi Han
Huijun Yuan
Jing Cheng
Kwong-Wai Choy
Liyang Liu
Michael Q Zhang
Pak C Sham
Xuegong Zhang
P2860
P304
P356
10.1111/AHG.12084
P407
P50
P577
2014-09-17T00:00:00Z