Fine-mapping and mutation analysis of TRPM1: A candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses

Briefings in Functional Genomics and Proteomics

Volumn 9, Issue 3, 2010, Pages 193-207

  Bellone, Rebecca R ^a   Forsyth, George ^b   Leeb, Tosso ^c   Archer, Sheila ^d   Sigurdsson, Snaevar ^d   Imsland, Freyja ^e   Mauceli, Evan ^d   Engensteiner, Martina ^c   Bailey, Ernest ^f   Sandmeyer, Lynne ^g   Grahn, Bruce ^g   Lindblad Toh, Kerstin ^d,e   Wade, Claire M ^h  

^a UNIVERSITY OF TAMPA   (United States)

^b UNIVERSITY OF SASKATCHEWAN   (Canada)

^c UNIVERSITY OF BERN   (Switzerland)

^d BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^e UPPSALA UNIVERSITY   (Sweden)

^f UNIVERSITY OF KENTUCKY   (United States)

^g UNIVERSITY OF SASKATCHEWAN   (Canada)

^h UNIVERSITY OF SYDNEY   (Australia)

Author keywords

Congenital stationary night blindness; Fine mapping; Illumina DNA sequencing; Leopard Complex spotting; Member I; Subfamily M; Transient receptor potential cation channel

Indexed keywords

TRANSIENT RECEPTOR POTENTIAL CHANNEL M1;

ARTICLE; CONGENITAL STATIONARY NIGHT BLINDNESS; CONTROLLED STUDY; DNA SEQUENCE; GENE MAPPING; GENETIC ASSOCIATION; GENOMICS; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HORSE DISEASE; LEOPARD COMPLEX SPOTTING; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; REGULATORY SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; DNA MUTATIONAL ANALYSIS; EXONS; GENETIC PREDISPOSITION TO DISEASE; HORSE DISEASES; HORSES; MOLECULAR SEQUENCE DATA; NIGHT BLINDNESS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; TRPM CATION CHANNELS;

EQUIDAE; MAMMALIA; PANTHERA PARDUS;

EID: 77953926968     PISSN: 14739550     EISSN: 14774062     Source Type: Journal    
DOI: 10.1093/bfgp/elq002     Document Type: Article

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