Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.
about
Diversity of the Genes Implicated in Algerian Patients Affected by Usher SyndromeStructure analyses reveal a regulated oligomerization mechanism of the PlexinD1/GIPC/myosin VI complexEPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing lossMutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.Genetic causes of moderate to severe hearing loss point to modifiers.Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
P2860
Q28553815-81C33E59-13B4-40B3-AB18-E72CDE80FAC3Q33769778-E4A4E373-667B-4D5D-AB45-F6E2DE8B9600Q35964651-D735CE10-8159-403F-8E69-8CD2EBA7698BQ38885154-F534285B-E353-4C35-A11E-92EA2E1ED598Q39442480-EA624193-28E2-4A33-BD20-E29C8383BDFDQ46809494-A5A508B2-8F7C-439D-B97A-B238A42351E7Q58803935-5084F51A-D338-4EA1-BF7C-0A2A52A96919
P2860
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Diversity of the causal genes ...... ied by whole exome sequencing.
@en
type
label
Diversity of the causal genes ...... ied by whole exome sequencing.
@en
prefLabel
Diversity of the causal genes ...... ied by whole exome sequencing.
@en
P2093
P2860
P50
P356
P1476
Diversity of the causal genes ...... ied by whole exome sequencing.
@en
P2093
Dominique Weil
Fatima Ammar-Khodja
Gaelle M Lefèvre
Hassina Ibrahim
Malek Louha
Malika Dahmani
Sofiane Ouhab
P2860
P304
P356
10.1002/MGG3.131
P577
2015-02-15T00:00:00Z