Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. [electronic resource]
Producer: 19990719Description: 300-4 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Anemia, Megaloblastic -- complications
- Animals
- Base Sequence
- Carrier Proteins -- genetics
- Cricetinae
- DNA -- genetics
- DNA Primers -- genetics
- Deafness -- complications
- Diabetes Complications
- Diabetes Mellitus -- genetics
- Female
- Genes, Recessive
- Genetic Markers
- Humans
- Male
- Membrane Transport Proteins
- Mice
- Molecular Sequence Data
- Mutation
- Physical Chromosome Mapping
- Sequence Homology, Amino Acid
- Syndrome
- Thiamine -- metabolism
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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