De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Detalles Bibliográficos
Autores principales: Yuan, Yongyi, Zhang, Jianguo, Chang, Qing, Zeng, Jin, Xin, Feng, Wang, Jianjun, Zhu, Qingyan, Wu, Jing, Lu, Jingqiao, Guo, Weiwei, Yan, Xukun, Jiang, Hui, Zhou, Binfei, Li, Qi, Gao, Xue, Yuan, Huijun, Yang, Shiming, Han, Dongyi, Mao, Zixu, Chen, Ping, Lin, Xi, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220163/
https://www.ncbi.nlm.nih.gov/pubmed/24913193
http://dx.doi.org/10.1038/cr.2014.77

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220163/
https://www.ncbi.nlm.nih.gov/pubmed/24913193
http://dx.doi.org/10.1038/cr.2014.77

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