ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss-Reference-Cited by-同舟云学术

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

Published:2018-04 Issue:4 Volume:137 Page:329-342
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Li Wu,Sun Jie,Ling Jie,Li Jiada,He Chufeng,Liu Yalan,Chen Hongsheng,Men Meichao,Niu Zhijie,Deng Yuyuan,Li Meng,Li Taoxi,Wen Jie,Sang Shushan,Li Haibo,Wan Zhengqing,Richard Elodie M.,Chapagain Prem,Yan Denise,Liu Xue Zhong,Mei Lingyun,Feng Yong

Funder

National Natural Science Foundation of China

the Major State Basic Research Development Program of China (973 Program)

National Institutes of Health/National Institute on Deafness and Other Communication Disorders

the China Postdoctoral Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/article/10.1007/s00439-018-1885-0/fulltext.html

Reference35 articles.

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4. Chakchouk I, Grati M, Bademci G, Bensaid M, Ma Q, Chakroun A, Foster J, Yan D, Duman D, Diaz-Horta O, Ghorbel A, Mittal R, Farooq A, Tekin M, Masmoudi S, Liu XZ (2015) Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Mol Genet Genom 290:1327–1334. https://doi.org/10.1007/s00438-015-0995-9

5. Chen H, Jiang L, Xie Z, Mei L, He C, Hu Z, Xia K, Feng Y (2010) Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome. Biochem Biophys Res Commun 397:70–74. https://doi.org/10.1016/j.bbrc.2010.05.066

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