A novel forkhead box C1 gene mutation in a Korean family with Axenfeld-Rieger syndrome.

Kim, Gyu-Nam; Ki, Chang-Seok; Seo, Seong-Wook; Yoo, Ji-Myong; Han, Yong-Seop; Chung, In-Young; Park, Jong-Moon; Kim, Seong-Jae

Kim, Gyu-Nam; Ki, Chang-Seok; Seo, Seong-Wook; Yoo, Ji-Myong; Han, Yong-Seop; Chung, In-Young; Park, Jong-Moon; Kim, Seong-Jae.

Affiliation

Kim GN; Department of Ophthalmology, Gyeongsang National University, College of Medicine, Jinju, Korea.

Mol Vis ; 19: 935-43, 2013.

Article in En | MEDLINE | ID: mdl-23687430

Subject(s)

Asian People/genetics; Eye Abnormalities/genetics; Forkhead Transcription Factors/genetics; Mutation/genetics; Adult; Anterior Eye Segment/abnormalities; Base Sequence; Child; DNA Mutational Analysis; Eye Abnormalities/pathology; Eye Diseases, Hereditary; Family; Female; Homeodomain Proteins/genetics; Humans; Infant, Newborn; Male; Molecular Sequence Data; Pedigree; Republic of Korea; Transcription Factors/genetics; Homeobox Protein PITX2

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Eye Abnormalities / Asian People / Forkhead Transcription Factors / Mutation Type of study: Prognostic_studies Limits: Adult / Child / Female / Humans / Male / Newborn Country/Region as subject: Asia Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2013 Type: Article

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