Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease

Human Genetics

Volumn 102, Issue 1, 1998, Pages 21-26

  Nasonkin, Igor ^a   Illing, Michelle ^a   Koehler, Michael R ^b   Schmid, Michael ^b   Molday, Robert S ^a   Weber, Bernhard H F ^b  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; COMPLEMENTARY DNA;

ANIMAL CELL; ARTICLE; CATTLE; CHROMOSOME 1P; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; GENE MUTATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RAT; RETINA ROD; STARGARDT DISEASE;

ANIMALIA; BOS TAURUS; BOVINAE;

EID: 0031922842     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050649     Document Type: Article

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