Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus

PURPOSE: To map and identify the genetic mutation underlying X-linked congenital nystagmus in a Chinese family. METHODS: Genomic DNA was prepared from peripheral blood, and linkage analysis was performed using short tandem repeat (STR) polymorphism markers. We used Cyrillic software to manage pedigr...

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Detalles Bibliográficos
Autores principales: Zhou, Pingtong, Wang, Zhiqiang, Zhang, Jing, Hu, Landian, Kong, Xiangyin
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408774/
https://www.ncbi.nlm.nih.gov/pubmed/18523664

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408774/
https://www.ncbi.nlm.nih.gov/pubmed/18523664

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