Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave

American Journal of Ophthalmology

Volumn 128, Issue 2, 1999, Pages 179-184

  Sieving, Paul A ^a   Bingham, Eve L ^a   Kemp, Jennifer ^a   Richards, Julia ^a   Hiriyanna, K ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; AGED; ARTICLE; B WAVE; CASE REPORT; DIAGNOSTIC APPROACH ROUTE; DIFFERENTIAL DIAGNOSIS; ELECTRORETINOGRAM; GENE MUTATION; HUMAN; MALE; MISSENSE MUTATION; NIGHT VISION; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; RETINOSCHISIS; SEQUENCE ANALYSIS; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADULT; ARGININE; DIAGNOSIS, DIFFERENTIAL; DNA; ELECTRORETINOGRAPHY; EXONS; EYE DISEASES, HEREDITARY; EYE PROTEINS; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; POLYMERASE CHAIN REACTION; RETINA; RETINAL DEGENERATION; TRYPTOPHAN; X CHROMOSOME;

EID: 0032777712     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(99)00144-0     Document Type: Article

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