Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations. [electronic resource]
Producer: 20110303Description: 6 p. digitalISSN:- 1471-2350
- Adenosine Triphosphatases -- genetics
- Adolescent
- Adult
- Alanine Transaminase -- analysis
- Asian People -- genetics
- Base Sequence
- Cation Transport Proteins -- genetics
- Ceruloplasmin -- analysis
- Child
- Child, Preschool
- Copper -- urine
- Copper-Transporting ATPases
- Exons
- Female
- Genetic Testing
- Hepatolenticular Degeneration -- diagnosis
- Homozygote
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Promoter Regions, Genetic
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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