Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease. [electronic resource]
Producer: 19980604Description: 275-8 p. digitalISSN:- 1059-7794
- Adenosine Triphosphatases -- genetics
- Alleles
- Base Sequence
- Carrier Proteins -- genetics
- Case-Control Studies
- Cation Transport Proteins
- Copper-Transporting ATPases
- DNA Primers -- genetics
- Gene Frequency
- Hepatolenticular Degeneration -- enzymology
- Humans
- Korea
- Mutation
- Point Mutation
- Polymerase Chain Reaction
- Polymorphism, Single-Stranded Conformational
- Sequence Deletion
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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