Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.

Xi, Quansheng; Pauer, Gayle J T; Traboulsi, Elias I; Hagstrom, Stephanie A

Xi, Quansheng; Pauer, Gayle J T; Traboulsi, Elias I; Hagstrom, Stephanie A.

Affiliation

Xi Q; Department of Ophthalmic Research, Cole Eye Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.

Exp Eye Res ; 83(3): 569-73, 2006 Sep.

Article in En | MEDLINE | ID: mdl-16643894

Subject(s)

Optic Atrophy, Hereditary, Leber/genetics; Proteins/genetics; Retinitis Pigmentosa/genetics; Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Case-Control Studies; Consanguinity; DNA Mutational Analysis; DNA Primers; Humans; Molecular Sequence Data; Mutation, Missense; Polymorphism, Single Nucleotide

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Retinitis Pigmentosa / Optic Atrophy, Hereditary, Leber Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Exp Eye Res Year: 2006 Type: Article Affiliation country: United States

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