Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness

Otoancorin (OTOA), encoded by OTOA, is required for the development of the tectorial membrane (TM) in the inner ear. Mutations in this gene cause non-syndromic hearing loss (DFNB22). The molecular mechanisms underlying most of DFNB22 remains poorly understood. Disruption of glycosylphosphatidylinosi...

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Detaylı Bibliyografya
Yayımlandı:Hum Mutat
Asıl Yazarlar: Kim, Bong Jik, Kim, Dong-Kyu, Han, Jin Hee, Oh, Jayoung, Kim, Ah Reum, Lee, Chung, Kim, Nayoung KD, Park, Hye-Rim, Kim, Min Young, Lee, Sejoon, Lee, Seungmin, Oh, Doo Yi, Park, Woong-Yang, Park, Sungjin, Choi, Byung Yoon
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2019
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6467692/
https://ncbi.nlm.nih.gov/pubmed/30740825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.23719
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