Molecular analysis of the rhodopsin gene in southern France: Identification of the first duplication responsible for retinitis pigmentosa, c.998 999ins4

Ophthalmic Genetics

Volumn 20, Issue 3, 1999, Pages 173-182

  Bareil, Corinne ^a   Hamel, Christian ^b   Pallarès Ruiz, Nathalie ^a   Arnaud, Bernard ^b   Demaille, Jacques ^a   Claustres, Mireille ^a,c  

^a INSTITUTE OF HUMAN GENETICS   (France)

^b MONTPELLIER UNIVERSITY HOSPITAL   (France)

^c Institute of Biology   (France)

Author keywords

Autosomal dominant retinitis pigmentosa; Rhodopsin mutations

Indexed keywords

RHODOPSIN; VISUAL PIGMENT;

ADULT; ARTICLE; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA FLANKING REGION; FEMALE; FRAMESHIFT MUTATION; FRANCE; GENE DUPLICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; MAJOR CLINICAL STUDY; MALE; PEDIGREE; PHOTORECEPTOR; PREVALENCE; PRIORITY JOURNAL; RETINA ROD; RETINITIS PIGMENTOSA;

EID: 0032725952     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/opge.20.3.173.2282     Document Type: Article

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