Oguchi disease: Phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene

Retina

Volumn 17, Issue 1, 1997, Pages 17-22

  Nakazawa, Mitsuru ^a   Wada, Yuko ^a   Fuchs, Sigrid ^b   Gal, Andreas ^b   Tamai, Makoto ^a  

^a TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; COLOR VISION; DARK ADAPTATION; FEMALE; GENE DELETION; GENE FREQUENCY; HOMOZYGOSITY; HUMAN; MALE; NIGHT BLINDNESS; SCREENING TEST; SINGLE STRAND CONFORMATION POLYMORPHISM; VISUAL ACUITY; VISUAL FIELD;

EID: 0031041746     PISSN: 0275004X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006982-199701000-00004     Document Type: Article

References (15)

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