RPE65 gene: multiplex PCR and mutation screening in patients from India with retinal degenerative diseases.

Joseph, Biju; Srinivasan, Anuradha; Soumittra, Nagasamy; Vidhya, Authiappan; Shetty, Nitin Sridhara; Uthra, Satagopan; Kumaramanickavel, Govindasamy

Joseph, Biju; Srinivasan, Anuradha; Soumittra, Nagasamy; Vidhya, Authiappan; Shetty, Nitin Sridhara; Uthra, Satagopan; Kumaramanickavel, Govindasamy.

Affiliation

Joseph B; Department of Genetics and Molecular Biology, Medical and Vision Research Foundations, Sankara Nethralaya, Chennai 600 006, India.

J Genet ; 81(1): 19-23, 2002 Apr.

Article in En | MEDLINE | ID: mdl-12357075

Subject(s)

Optic Atrophy, Hereditary, Leber/genetics; Proteins/genetics; Retinitis Pigmentosa/genetics; Carrier Proteins; DNA Mutational Analysis; Eye Proteins; Female; Genetic Testing; Humans; India; Male; Pedigree; Polymerase Chain Reaction; cis-trans-Isomerases

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Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Retinitis Pigmentosa / Optic Atrophy, Hereditary, Leber Type of study: Diagnostic_studies / Screening_studies Limits: Female / Humans / Male Country/Region as subject: Asia Language: En Journal: J Genet Year: 2002 Type: Article Affiliation country: India

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