Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.

Hutcheson, Kelly A; Paluru, Prasuna C; Bernstein, Steven L; Koh, Jamie; Rappaport, Eric F; Leach, Richard A; Young, Terri L

Hutcheson, Kelly A; Paluru, Prasuna C; Bernstein, Steven L; Koh, Jamie; Rappaport, Eric F; Leach, Richard A; Young, Terri L.

Affiliation

Hutcheson KA; Department of Ophthalmology, Children's National Medical Center, Washington, DC, USA.

Mol Vis ; 11: 501-8, 2005 Jul 14.

Article in En | MEDLINE | ID: mdl-16052165

Subject(s)

Black or African American/genetics; Eye Proteins/genetics; Nerve Tissue Proteins/genetics; Polymorphism, Genetic; Retinopathy of Prematurity/ethnology; Retinopathy of Prematurity/genetics; White People/genetics; 3' Untranslated Regions/genetics; 5' Untranslated Regions/genetics; Adult; Case-Control Studies; Cohort Studies; DNA Transposable Elements; Exons; Female; Gene Deletion; Heterozygote; Humans; Infant, Newborn; Male; Polymorphism, Single Nucleotide; Retinopathy of Prematurity/physiopathology; Severity of Illness Index

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Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Black or African American / Retinopathy of Prematurity / White People / Eye Proteins / Nerve Tissue Proteins Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Newborn Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2005 Document type: Article Affiliation country: United States

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