Yüklüyor......

Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis

PURPOSE: Usher syndrome accounts for about 50% of all hereditary deaf-blindness cases. The most severe form of this syndrome, Usher syndrome type I (USH1), is characterized by profound congenital sensorineural deafness, vestibular dysfunction, and retinitis pigmentosa. Six USH1 genes have been ident...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Mol Vis
Asıl Yazarlar: Ben-Rebeh, Imen, Grati, Mhamed, Bonnet, Crystel, Bouassida, Walid, Hadjamor, Imen, Ayadi, Hammadi, Ghorbel, Abdelmonem, Petit, Christine, Masmoudi, Saber
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Molecular Vision 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4950652/
https://ncbi.nlm.nih.gov/pubmed/27440999
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!