R778L, H1069Q, and I1102T mutation study in neurologic Wilson disease. [electronic resource]
Producer: 20101026Description: 627-30 p. digitalISSN:- 0028-3886
- Adenosine Triphosphatases -- genetics
- Adolescent
- Adult
- Amino Acids -- genetics
- Cation Transport Proteins -- genetics
- Child
- Child, Preschool
- Copper-Transporting ATPases
- DNA Mutational Analysis -- methods
- Family Health
- Female
- Gene Frequency
- Hepatolenticular Degeneration -- genetics
- Humans
- India
- Magnetic Resonance Imaging -- methods
- Male
- Mutation -- genetics
- Severity of Illness Index
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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