Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. [electronic resource]
Producer: 20130827Description: e57195 p. digitalISSN:- 1932-6203
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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