Novel OTX2 mutation associated with congenital anophthalmia and microphthalmia in a Han Chinese family

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Bibliographic Details
Published inActa ophthalmologica (Oxford, England) Vol. 90; no. 6; pp. e501 - e502
Main Authors You, Tian, Lv, Yuan, Liu, Shuqun, Li, Fei, Zhao, Yan, Lv, Jingyu, Qiu, Guangrong, Li-Ling, Jesse
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.09.2012
Subjects
Anophthalmos - genetics
Asian Continental Ancestry Group - genetics
Child
China - epidemiology
Family Health
Female
Humans
Magnetic Resonance Imaging
Male
Microphthalmos - genetics
Middle Aged
Mutation
Otx Transcription Factors - genetics
China
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Bibliography:ark:/67375/WNG-PC0VK7VS-B
istex:D79F4460A308CFE6CDC14212B3471FFC070F497E
ArticleID:AOS2345
Authors who have contributed equally to this study.
content type line 23
SourceType-Scholarly Journals-1
ObjectType-Correspondence-1
ISSN:1755-375X
1755-3768
1755-3768
DOI:10.1111/j.1755-3768.2011.02345.x