Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed

PLoS Genetics

Volumn 8, Issue 1, 2012, Pages

  Forman, Oliver P ^a   Penderis, Jacques ^b   Hartley, Claudia ^a   Hayward, Louisa J ^a   Ricketts, Sally L ^a   Mellersh, Cathryn S ^a  

^a ANIMAL HEALTH TRUST   (United Kingdom)

^b UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BCAN GENE; CHROMOSOME 13; CHROMOSOME 7; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA SEQUENCE; DOG; DOMESTIC ANIMAL; DRY EYE; EPISODIC FALLING; EXON; FAMILY WITH SEQUENCE SIMILARITY 83 MEMBER H GENE; GENE DELETION; GENE FUNCTION; GENE MAPPING; GENE TARGETING; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC VARIABILITY; KERATOCONJUNCTIVITIS SICCA; MUSCLE HYPERTONIA; MUTATOR GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; SIGNAL TRANSDUCTION; ANIMAL; ANIMAL DISEASE; BREEDING; CHROMOSOME MAP; DOG DISEASE; GENETIC PREDISPOSITION; GENETICS; METHODOLOGY; MOLECULAR GENETICS; SINGLE NUCLEOTIDE POLYMORPHISM; SKIN DISEASE;

CANIS FAMILIARIS;

ANIMALS; BASE SEQUENCE; BREEDING; CHROMOSOME MAPPING; DOG DISEASES; DOGS; EXONS; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; MOLECULAR SEQUENCE DATA; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; SKIN DISEASES;

EID: 84857491696     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1002462     Document Type: Article

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