Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions
about
DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes.Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in SiberiaDiagnostic pitfalls for -related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss
P2860
Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Update of the GJB2/DFNB1 mutat ...... nt among other large deletions
@en
type
label
Update of the GJB2/DFNB1 mutat ...... nt among other large deletions
@en
prefLabel
Update of the GJB2/DFNB1 mutat ...... nt among other large deletions
@en
P2093
P2860
P50
P356
P1476
Update of the GJB2/DFNB1 mutat ...... nt among other large deletions
@en
P2093
Alexander V Polyakov
Elena K Kudryashova
Elena V Balanovska
Maria R Lalayants
Natalya V Nikitina
Oleg P Balanovsky
Roza A Skhalyakho
Sergey V Voronin
Tatiana G Markova
P2860
P2888
P304
P356
10.1038/JHG.2017.42
P577
2017-04-13T00:00:00Z