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A novel GPR143 duplication mutation in a Chinese family with X-linked congenital nystagmus

PURPOSE: To elucidate the molecular genetic defect of X-linked congenital nystagmus in a Chinese family. METHODS: Genomic DNA was prepared from peripheral blood. We used allele-sharing analysis to identify the possible locus harboring the disease-causing gene. We screened for mutations in the G prot...

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Main Authors: Peng, Yuanyuan, Meng, Yan, Wang, Zheng, Qin, Mei, Li, Xiaoqiao, Dian, Yan, Huang, Shangzhi
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2671585/
https://ncbi.nlm.nih.gov/pubmed/19390656
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