Low frequency of rhodopsin mutations in South African patients with autosomal dominant retinitis pigmentosa

Clinical Genetics

Volumn 58, Issue 1, 2000, Pages 77-78

  Roberts, L ^a   Ramesar, R ^a   Greenberg, J ^a  

^a UNIVERSITY OF CAPE TOWN   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

RHODOPSIN;

AUTOSOMAL DOMINANT INHERITANCE; HUMAN; LETTER; MAJOR CLINICAL STUDY; MUTATION RATE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SOUTH AFRICA;

AMINO ACID SUBSTITUTION; CODON; DNA MUTATIONAL ANALYSIS; GENES, DOMINANT; HUMANS; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RETINITIS PIGMENTOSA; RHODOPSIN; SOUTH AFRICA;

EID: 0033910921     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2000.580114.x     Document Type: Letter

References (0)