Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa [1]

British Journal of Ophthalmology

Volumn 82, Issue 6, 1998, Pages 709-

  Simonelli, F ^a   Rinaldi, M ^a   Nesti, A ^a   Testa, F ^a   Rinaldi, E ^a   Ciccodicola, A ^a   Flagiello, L ^a   Giuseppina Miano, M ^a   D'Urso, M ^a  

^a SECOND UNIVERSITY OF NAPLES   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

RHODOPSIN;

ADULT; AMINO ACID SUBSTITUTION; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHILD; COLOR VISION; FEMALE; GENE MUTATION; GENE SEGREGATION; HUMAN; LETTER; MALE; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; VISUAL ACUITY; VISUAL FIELD;

EID: 17644441280     PISSN: 00071161     EISSN: None     Source Type: Journal    
DOI: 10.1136/bjo.82.6.709     Document Type: Letter

References (4)