Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3

Genomics

Volumn 48, Issue 3, 1998, Pages 341-345

  Finckh, Ulrich ^a   Xu, Suying ^a   Kumaramanickavel, Govindasamy ^b   Schürmann, Manfred ^c   Mukkadan, J K ^d   Fernandez, S Tony ^d   John, Sheila ^b   Weber, James L ^e   Denton, Michael J ^f   Gal, Andreas ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b MEDICAL RESEARCH FOUNDATION   (India)

^c UNIVERSITY OF LÜBECK   (Germany)

^d Little Flower Med Research Center   (India)

^e MARSHFIELD CLINIC   (United States)

^f UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA CHAIN; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 16P; DEGENERATIVE DISEASE; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA;

EID: 0032521129     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5194     Document Type: Article

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