ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients. [electronic resource]
Producer: 20070320Description: 277-82 p. digitalISSN:- 0254-8860
- Adenosine Triphosphatases -- genetics
- Adolescent
- Adult
- Age of Onset
- Cation Transport Proteins -- genetics
- Ceruloplasmin -- analysis
- Child
- Codon
- Consanguinity
- Copper -- urine
- Copper-Transporting ATPases
- Exons
- Female
- Hepatolenticular Degeneration -- genetics
- Humans
- India
- Male
- Middle Aged
- Mutation
- Phenotype
- Polymorphism, Genetic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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