FOXF2 is required for cochlear development in humans and mice

Molecular mechanisms governing the development of the human cochlea remain largely unknown. Through genome sequencing, we identified a homozygous FOXF2 variant c.325A>T (p.I109F) in a child with profound sensorineural hearing loss (SNHL) associated with incomplete partition type I anomaly of the...

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Библиографические подробности
Опубликовано в: :Hum Mol Genet
Главные авторы: Bademci, Guney, Abad, Clemer, Incesulu, Armagan, Elian, Fahed, Reyahi, Azadeh, Diaz-Horta, Oscar, Cengiz, Filiz B, Sineni, Claire J, Seyhan, Serhat, Atli, Emine Ikbal, Basmak, Hikmet, Demir, Selma, Nik, Ali Moussavi, Footz, Tim, Guo, Shengru, Duman, Duygu, Fitoz, Suat, Gurkan, Hakan, Blanton, Susan H, Walter, Michael A, Carlsson, Peter, Walz, Katherina, Tekin, Mustafa
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2019
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General Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6452198/
https://ncbi.nlm.nih.gov/pubmed/30561639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy431
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