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dc.contributor.authorChen, Suqinzh_CN
dc.contributor.authorZhang, Yanlingzh_CN
dc.contributor.authorWang, Yimingzh_CN
dc.contributor.authorLi, Weilizh_CN
dc.contributor.authorHuang, Shuangzh_CN
dc.contributor.authorChu, Xinzh_CN
dc.contributor.authorWang, Leizh_CN
dc.contributor.authorZhang, Meizh_CN
dc.contributor.authorLiu, Zuguozh_CN
dc.contributor.author王艺明zh_CN
dc.date.accessioned2013-12-12T02:20:53Z
dc.date.available2013-12-12T02:20:53Z
dc.date.issued2007-01zh_CN
dc.identifier.citationAmerican Journal of Ophthalmology, 2007,143(1):186-188zh_CN
dc.identifier.issn0002-9394zh_CN
dc.identifier.otherISI:000243311700042zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/64880
dc.description.abstractPURPOSE: To investigate the genetic findings and phenotypic characters of autosomal dominant optic atrophy (ADOA). DESIGN: Case report and experimental study. METHODS: Molecular genetic analysis and clinical examinations were performed in a Chinese family with ADOA. Mutations in OPA1 were detected by direct sequencing. Haplotypes were constructed and compared with the phenotypes in the family. RESULTS: Nine family members were diagnosed with ADOA and some of them were accompanied with hearing loss and/or high myopia. A novel heterozygous mutation, c.2848_2849delGA(p.Asp950CysfsX4), was detected in all ADOA patients. The mutation and the mutation bearing haplotype cosegregated with the nine affected members. One family member had high myopia without vision or hearing loss. This patient along with unaffected ones did not harbor the mutation. CONCLUSIONS: A novel mutation, c.2848_2849delGA in OPA1, was identified in a Chinese family with ADOA. This mutation is associated with hearing loss, but likely not high myopia.zh_CN
dc.language.isoen_USzh_CN
dc.source.urihttp://dx.doi.org/10.1016/j.ajo.2006.06.049zh_CN
dc.subjectGENEzh_CN
dc.titleA novel OPA1 mutation responsible for autosomal dominant optic atrophy with high frequency hearing loss in a Chinese familyzh_CN
dc.typeArticlezh_CN


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