Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation. [electronic resource]
Producer: 20081218Description: 273-8 p. digitalISSN:- 1089-8646
- Amino Acid Sequence
- Animals
- Brazil
- Chromosome Mapping
- Chromosomes, Human, Pair 13 -- genetics
- Female
- Genes, Recessive
- Genetic Linkage
- Genetic Predisposition to Disease
- Humans
- Hypotrichosis -- genetics
- Lod Score
- Male
- Mice
- Models, Molecular
- Molecular Sequence Data
- Mutation
- Pedigree
- Polymorphism, Single Nucleotide
- Receptors, Purinergic P2 -- genetics
- Sequence Analysis, DNA
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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