Yüklüyor......

Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family

Hereditary nonsyndromic hearing loss is highly heterogeneous and most patients with a presumed genetic etiology lack a specific diagnosis. It has been estimated that several hundred genes may be associated with this sensory deficit in humans. Here, we identified compound heterozygous mutations in th...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Gao, Xue, Su, Yu, Guan, Li-Ping, Yuan, Yong-Yi, Huang, Sha-Sha, Lu, Yu, Wang, Guo-Jian, Han, Ming-Yu, Yu, Fei, Song, Yue-Shuai, Zhu, Qing-Yan, Wu, Jing, Dai, Pu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3653921/
https://ncbi.nlm.nih.gov/pubmed/23690975
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0063026
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!