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OPTINEURIN SEQUENCE VARIANTS IN BRITISH GLAUCOMA SUBJECTS 被引量:2
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作者 T.Aung N.Ebenezer +4 位作者 G.Brice a.child R.Hitchings O.Lehmann S.Bhattacharya 《国际眼科杂志》 CAS 2003年第1期97-98,共2页
Aim: A recent study found that the Optineurin (OPTN) gene was mutated in families with primary open angle glaucoma (POAG), A misense mutation E50K was present in 13.5% of families studied, and the M98K risk-associated... Aim: A recent study found that the Optineurin (OPTN) gene was mutated in families with primary open angle glaucoma (POAG), A misense mutation E50K was present in 13.5% of families studied, and the M98K risk-associated change was identified in 13.6% of POAG subjects. The aim of this study was to investi- 展开更多
关键词 青光眼 英国患者 OPTINEURIN 基因突变 POAG
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