Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness
about
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss.Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patientsMutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.Comorbidity in the Tunisian population.Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.Identification of four TMC1 variations in different Chinese families with hereditary hearing loss.Genetics and genomic medicine in Tunisia.
P2860
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P2860
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness
description
2014 nî lūn-bûn
@nan
2014 թուականին հրատարակուած գիտական յօդուած
@hyw
2014 թվականին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Whole exome sequencing identif ...... es with non-syndromic deafness
@ast
Whole exome sequencing identif ...... es with non-syndromic deafness
@en
Whole exome sequencing identif ...... es with non-syndromic deafness
@en-gb
Whole exome sequencing identif ...... es with non-syndromic deafness
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type
label
Whole exome sequencing identif ...... es with non-syndromic deafness
@ast
Whole exome sequencing identif ...... es with non-syndromic deafness
@en
Whole exome sequencing identif ...... es with non-syndromic deafness
@en-gb
Whole exome sequencing identif ...... es with non-syndromic deafness
@nl
altLabel
Whole Exome Sequencing Identif ...... es with Non-Syndromic Deafness
@en
prefLabel
Whole exome sequencing identif ...... es with non-syndromic deafness
@ast
Whole exome sequencing identif ...... es with non-syndromic deafness
@en
Whole exome sequencing identif ...... es with non-syndromic deafness
@en-gb
Whole exome sequencing identif ...... es with non-syndromic deafness
@nl
P2093
P2860
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P1476
Whole exome sequencing identif ...... es with non-syndromic deafness
@en
P2093
Dominique Weil
Ghazi Besbes
Imen Dorboz
Jacqueline Levilliers
Kenneth McElreavey
Laurence Jonard
Malek Louha
Mariem Chargui
Nadia Laroussi
Odile Tanguy Boespflug
P2860
P304
P356
10.1371/JOURNAL.PONE.0099797
P407
P577
2014-01-01T00:00:00Z