A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
about
The unique electrical properties in an extracellular fluid of the mammalian cochlea; their functional roles, homeostatic processes, and pathological significance.Navigating genetic diagnostics in patients with hearing loss.Recent Advancements in the Regeneration of Auditory Hair Cells and Hearing RestorationGenetics and genomic medicine in Tunisia.
P2860
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
description
2016 nî lūn-bûn
@nan
2016 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մարտին 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
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@ast
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@en
type
label
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@ast
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@en
prefLabel
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@ast
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@en
P2093
P2860
P50
P1433
P1476
A mutation in SLC22A4 encoding ...... -syndromic hearing loss DFNB60
@en
P2093
Abdelmonem Ghorbel
Denise Yan
Imen Chakchouk
Lingling Neng
Mounira Hmani
Rahul Mittal
Saber Masmoudi
P2860
P2888
P304
P356
10.1007/S00439-016-1657-7
P577
2016-03-29T00:00:00Z
P5875
P6179
1010092107