Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC)

Cytogenetics and Cell Genetics

Volumn 73, Issue 1-2, 1996, Pages 81-85

  Van Soest, S ^a   Te Nijenhuis, S ^a   Van Den Born, L I ^a,b   Bleeker Wagemakers, E M ^a   Sharp, E ^c   Sandkuijl, L A ^b   Westerveld, A ^d   Bergen, A A B ^a  

^a NETHERLANDS INSTITUTE FOR NEUROSCIENCE   (Netherlands)

^b ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^c TRINITY COLLEGE DUBLIN   (Ireland)

^d UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

PHOSDUCIN;

ARTICLE; CHROMOSOME 1Q; FEMALE; GENE MAPPING; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; MARKER GENE; NETHERLANDS; PEDIGREE ANALYSIS; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINITIS PIGMENTOSA;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 1; EYE PROTEINS; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; GTP-BINDING PROTEIN REGULATORS; HAPLOTYPES; HUMANS; LOD SCORE; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; PHOSPHOPROTEINS; RETINITIS PIGMENTOSA;

EID: 0029893291     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134313     Document Type: Article

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