c-Ret–mediated hearing loss in mice with Hirschsprung disease

A significantly increased risk for dominant sensorineural deafness in patients who have Hirschsprung disease (HSCR) caused by endothelin receptor type B and SOX10 has been reported. Despite the fact that c-RET is the most frequent causal gene of HSCR, it has not been determined whether impairments o...

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Detaylı Bibliyografya
Asıl Yazarlar: Ohgami, Nobutaka, Ida-Eto, Michiru, Shimotake, Takashi, Sakashita, Naomi, Sone, Michihiko, Nakashima, Tsutomu, Tabuchi, Keiji, Hoshino, Tomofumi, Shimada, Atsuyoshi, Tsuzuki, Toyonori, Yamamoto, Masahiko, Sobue, Gen, Jijiwa, Mayumi, Asai, Naoya, Hara, Akira, Takahashi, Masahide, Kato, Masashi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2010
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2919946/
https://ncbi.nlm.nih.gov/pubmed/20616061
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1004520107
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