Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy.
Vernau, Karen M
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. [electronic resource] - PloS one 2013 - e57195 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0057195 doi
Animals
Base Sequence
Biological Transport--genetics
Brain Diseases, Metabolic--genetics
Dog Diseases--genetics
Dogs
Exons
Female
Genetic Loci
Genome-Wide Association Study
Heterozygote
Homozygote
Humans
Leigh Disease--genetics
Male
Membrane Transport Proteins--genetics
Molecular Sequence Data
Mutation
Polymorphism, Single Nucleotide
Thiamine--metabolism
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. [electronic resource] - PloS one 2013 - e57195 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1932-6203
10.1371/journal.pone.0057195 doi
Animals
Base Sequence
Biological Transport--genetics
Brain Diseases, Metabolic--genetics
Dog Diseases--genetics
Dogs
Exons
Female
Genetic Loci
Genome-Wide Association Study
Heterozygote
Homozygote
Humans
Leigh Disease--genetics
Male
Membrane Transport Proteins--genetics
Molecular Sequence Data
Mutation
Polymorphism, Single Nucleotide
Thiamine--metabolism