Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus

OBJECTIVES: Infantile nystagmus (IN) is a genetically heterogeneous condition characterised by involuntary rhythmic oscillations of the eyes accompanied by different degrees of vision impairment. Two genes have been identified as mainly causing IN: FRMD7 and GPR143. The aim of our study was to ident...

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Detalles Bibliográficos
Autores principales: Zhao, Hui, Huang, Xiu-Feng, Zheng, Zhi-Li, Deng, Wen-Li, Lei, Xin-Lan, Xing, Dong-Jun, Ye, Liang, Xu, Su-Zhong, Chen, Jie, Zhang, Fang, Yu, Xin-Ping, Jin, Zi-Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Ophthalmology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823450/
https://www.ncbi.nlm.nih.gov/pubmed/27036142
http://dx.doi.org/10.1136/bmjopen-2015-010649

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823450/
https://www.ncbi.nlm.nih.gov/pubmed/27036142
http://dx.doi.org/10.1136/bmjopen-2015-010649

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