Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss.
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Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss.
description
2017 nî lūn-bûn
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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
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2017年學術文章
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name
Identification of a rare COCH ...... inant late-onset hearing loss.
@en
type
label
Identification of a rare COCH ...... inant late-onset hearing loss.
@en
prefLabel
Identification of a rare COCH ...... inant late-onset hearing loss.
@en
P2093
P2860
P50
P1476
Identification of a rare COCH ...... inant late-onset hearing loss.
@en
P2093
Alexandra Frohne
Andreas Kirchnawy
Berthold Streubel
Klemens Frei
Martin Koenighofer
Wolfgang Gstoettner
P2860
P2888
P304
P356
10.1007/S00508-017-1230-Y
P577
2017-07-21T00:00:00Z
P6179
1090851650