Leber congenital amaurosis and retinitis pigmentosa with coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene

American Journal of Human Genetics

Volumn 69, Issue 1, 2001, Pages 198-203

  Den Hollander, Anneke I ^a   Heckenlively, John R ^c   van den Born, L Ingeborgh ^d   De Kok, Yvette J M ^a   Van der Velde Visser, Saskia D ^a   Kellner, Ulrich ^e   Jurklies, Bernhard ^f   Van Schooneveld, Mary J ^g,h   Blankenagel, Anita ^h   Rohrschneider, Klaus ^h   Wissinger, Bernd ⁱ   Cruysberg, Johan R M ^b   Deutman, August F ^b   Brunner, Han G ^a   Apfelstedt Sylla, Eckart ⁱ   Hoyng, Carel B ^b   Cremers, Frans P M ^a  

^a University Medical Centre Nijmege   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d ROTTERDAM EYE HOSPITAL   (Netherlands)

^e CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^f UNIVERSITY HOSPITAL ESSEN   (Germany)

^g UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^h UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

ⁱ UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALTERNATIVE RNA SPLICING; ARTICLE; DISEASE ASSOCIATION; ENVIRONMENTAL FACTOR; GENE MUTATION; GERMANY; HEREDITY; HUMAN; LEBER CONGENITAL AMAUROSIS; MAJOR CLINICAL STUDY; NETHERLANDS; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RECESSIVE INHERITANCE; RETINA DETACHMENT; RETINITIS PIGMENTOSA; RISK FACTOR; SIBLING; UNITED STATES; VASCULAR DISEASE; VISUAL FIELD; VISUAL IMPAIRMENT;

EID: 0034964652     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/321263     Document Type: Article

References (22)

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