Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus

Ophthalmology

Volumn 108, Issue 8, 2001, Pages 1479-1484

  Driessen, Carola A G G ^a   Janssen, Bert P M ^a   Winkens, Huub J ^a   Kuhlmann, Leonoor D ^a   Van Vugt, Anke H M ^a   Pinckers, Alfred J L G ^a   Deutman, August F ^a   Janssen, Jacques J M ^a  

^a RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOL DEHYDROGENASE;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA HYBRIDIZATION; EXON; EYE FUNDUS ALBIPUNCTATUS; FRAMESHIFT MUTATION; GENE INSERTION; GENE MUTATION; GENETIC DISORDER; HUMAN; MISSENSE MUTATION; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RETINA DISEASE;

ADULT; ALCOHOL OXIDOREDUCTASES; BASE SEQUENCE; CASE-CONTROL STUDIES; CHILD; DNA MUTATIONAL ANALYSIS; EXONS; EYE DISEASES, HEREDITARY; FEMALE; FUNDUS OCULI; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; NIGHT BLINDNESS; NUCLEIC ACID HYBRIDIZATION; PEDIGREE;

EID: 0034896040     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(01)00640-6     Document Type: Article

References (27)

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