Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations

Investigative Ophthalmology and Visual Science

Volumn 43, Issue 9, 2002, Pages 3027-3036

  Berson, Eliot L ^a   Rosner, Bernard ^a   Weigel DiFranco, Carol ^a   Dryja, Thaddeus P ^a   Sandberg, Michael A ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RHODOPSIN;

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CARBOXY TERMINAL SEQUENCE; CHILD; DIAGNOSTIC ACCURACY; DISEASE COURSE; ELECTRORETINOGRAPHY; FEMALE; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RETINA DEGENERATION; RETINITIS PIGMENTOSA; STATISTICAL ANALYSIS; VISUAL FIELD DEFECT; VISUAL IMPAIRMENT;

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; CHILD; DISEASE PROGRESSION; ELECTRORETINOGRAPHY; FEMALE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; RETINITIS PIGMENTOSA; RHODOPSIN; VISUAL ACUITY; VISUAL FIELDS;

EID: 0036725693     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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