A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family-Reference-Cited by-同舟云学术

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Published:2018-03-20 Issue:6 Volume:63 Page:723-730
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Deng Yuyuan,Niu Zhijie,Fan LiangLiang,Ling Jie,Chen Hongsheng,Cai Xinzhang,Mei Lingyun,He Chufeng,Zhang Xuewei,Wen Jie,Li Meng,Li Wu,Li Taoxi,Sang Shushan,Liu Yalan,Feng Yong

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s10038-018-0443-x.pdf

Reference23 articles.

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2. Petersen MB, Wang Q, Willems PJ. Sex-linked deafness. Clin Genet. 2008;73:14–23.

3. Dobyns WB. The pattern of inheritance of X-linked traits is not dominant or recessive, just X-linked. Acta Paediatr Suppl. 2006;95:11–5.

4. Mittal R, Patel K, Mittal J, Chan B, Yan D, Grati M, et al. Association of PRPS1 mutations with disease phenotypes. Dis Markers. 2015;2015:127013.

5. de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, et al. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science. 1995;267:685–8.

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