Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1).
about
A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73.Three-Category Classification of Magnetic Resonance Hearing Loss Images Based on Deep Autoencoder.Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing lossPhenotype description and response to thrombopoietin receptor agonist in -related disorder
P2860
Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1).
description
2016 nî lūn-bûn
@nan
2016 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@ast
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@en
type
label
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@ast
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@en
prefLabel
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@ast
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@en
P2093
P2860
P356
P1433
P1476
Extension of the clinical and ...... dominant hearing loss (DFNA1).
@en
P2093
R Lang-Roth
T Eisenberger
U Zimmermann
P2860
P304
P356
10.1111/CGE.12915
P577
2016-11-03T00:00:00Z