Genotyping Microarray (Gene Chip) for the ABCR (ABCA4) Gene

Human Mutation

Volumn 22, Issue 5, 2003, Pages 395-403

  Jaakson, K ^a   Zernant, J ^a,b   Kulm M ^a   Hutchinson, A ^b   Tonisson, N ^a   Glavac D ^c   Ravnik Glavac M ^c,d   Hawlina, M ^e   Meltzer, M R ^f   Caruso, R C ^f   Testa, F ^g   Maugeri, A ^h   Hoyng, C B ^h   Gouras, P ^b   Simonelii, F ^g   Lewis, R A ⁱ   Lupski, J R ⁱ   Cremers, F P M ^h   Allikmets, Rando ^b  

^a Asper Biotech Ltd   (Estonia)

^b Och Spine at New York Presbyterian Hospitals   (United States)

^c INSTITUTE OF PATHOLOGY   (Slovenia)

^d UNIVERSITY OF LJUBLJANA   (Slovenia)

^e UNIVERSITY MEDICAL CENTRE LJUBLJANA   (Slovenia)

^f NATIONAL EYE INSTITUTE   (United States)

^g SECOND UNIVERSITY OF NAPLES   (Italy)

^h RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

ⁱ BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

ABCA4; ABCR; Genotyping; Microarray; Mutation detection; Mutation screening; Stargardt disease; STGD1

Indexed keywords

OLIGONUCLEOTIDE;

ALLELE; ARTICLE; CONTROLLED STUDY; DNA MICROARRAY; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; VALIDATION PROCESS;

ATP-BINDING CASSETTE TRANSPORTERS; DNA MUTATIONAL ANALYSIS; GENOTYPE; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, GENETIC; REPRODUCIBILITY OF RESULTS; RETINAL DISEASES; VARIATION (GENETICS);

EID: 10744227207     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10263     Document Type: Article

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