OPA1 plus phenotypic variation in dominantly inherited optic atrophy attributable to genetic background

被引：0

作者：

Joanna, Poulton ^{[1
]}

Morten, K. ^{[1
]}

Williams, A. ^{[2
]}

Fearnley, I. ^{[3
]}

Rosser, L. ^{[4
]}

Lowndes, J. ^{[5
]}

Ashley, N. ^{[1
]}

Fratter, C. ^{[6
]}

Votruba, M. ^{[7
]}

机构：

[1] Womens Ctr, Nuffield Dept Obstet & Gynaecol, Oxford, England

[2] Northampton Gen Hosp, Dept Paediat, Northampton, England

[3] Northampton Gen Hosp, Dept Opthalmol, Northampton, England

[4] Univ Wales Hosp, Inst Med Genet, Cardiff CF4 4XW, S Glam, Wales

[5] Churchill Hosp, Dept Clin Genet, Oxford, England

[6] Churchill Hosp, Mol Genet Labs, Oxford, England

[7] Cardiff Univ, Sch Optometry & Vis Sci, Cardiff, S Glam, Wales

来源：

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：S89 / S89

页数：1