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pubmed-article:19862333pubmed:abstractTextMutations in the glutamate receptor metabotropic 6 gene (GRM6) have been identified in patients with congenital stationary night blindness (CSNB1B). High myopia is usually observed in CSNB1B patients. This study tested if any mutations in GRM6 were solely responsible for high myopia.lld:pubmed
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pubmed-article:19862333pubmed:authorpubmed-author:ZhangQingjion...lld:pubmed
pubmed-article:19862333pubmed:authorpubmed-author:XiaoXueshanXlld:pubmed
pubmed-article:19862333pubmed:authorpubmed-author:GuoXiangmingXlld:pubmed
pubmed-article:19862333pubmed:authorpubmed-author:LiShiqiangSlld:pubmed
pubmed-article:19862333pubmed:authorpubmed-author:WangPanfengPlld:pubmed
pubmed-article:19862333pubmed:authorpubmed-author:XuXiaoyuXlld:pubmed
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pubmed-article:19862333pubmed:dateRevised2010-9-28lld:pubmed
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pubmed-article:19862333pubmed:year2009lld:pubmed
pubmed-article:19862333pubmed:articleTitleSequence variations of GRM6 in patients with high myopia.lld:pubmed
pubmed-article:19862333pubmed:affiliationState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.lld:pubmed
pubmed-article:19862333pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19862333pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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