Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy

American Journal of Human Genetics

Volumn 67, Issue 4, 2000, Pages 960-966

  Maugeri, Alessandra ^a   Klevering, B Jeroen ^a   Rohrschneider, Klaus ^b   Blankenagel, Anita ^b   Brunner, Han G ^a   Deutman, August F ^a   Hoyng, Carel B ^a   Cremers, Frans P M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER;

ARTICLE; CLINICAL ARTICLE; DNA SEQUENCE; GENE ISOLATION; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HUMAN; OPHTHALMOSCOPY; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RETINA CONE; RETINA DYSTROPHY; RETINA ROD; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0033794939     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303079     Document Type: Article

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