The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
about
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.Novel deletions involving the USH2A gene in patients with Usher syndrome and retinitis pigmentosa.An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patientsA QSAR, pharmacokinetic and toxicological study of new artemisinin compounds with anticancer activity.A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II.
P2860
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
@ast
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
@en
type
label
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
@ast
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
@en
prefLabel
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
@ast
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
@en
P2093
P2860
P1433
P1476
The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort
@en
P2093
Anne-Françoise Roux
Christel Vaché
Elena Aller
Gema García-García
Jose M Millan
Mireille Claustres
Sue Malcolm
P2860
P304
P356
10.3390/MOLECULES19010367
P577
2013-02-13T00:00:00Z