Novel mutations of FRMD7 in Chinese patients with congenital motor nystagmus

The purpose of the current study was to identify novel mutations in the FRMD7 (FERM domain containing 7) gene and to characterize clinical features in Chinese patients with congenital motor nystagmus. For this purpose, 18 patients with congenital motor nystagmus were selected from the ocular genetic...

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Detalles Bibliográficos
Autores principales: Jia, Xiuhua, Zhu, Xiang, Li, Qigen, Jia, Xiaoyun, Li, Shiqiang, Guo, Xiangming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562100/
https://www.ncbi.nlm.nih.gov/pubmed/28656292
http://dx.doi.org/10.3892/mmr.2017.6824

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562100/
https://www.ncbi.nlm.nih.gov/pubmed/28656292
http://dx.doi.org/10.3892/mmr.2017.6824

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