Gene mutations in Wilson disease in Egyptian children: report on two novel mutations. [electronic resource]
Producer: 20160107Description: 114-8 p. digitalISSN:- 2090-2387
- Adenosine Triphosphatases -- genetics
- Adolescent
- Cation Transport Proteins -- genetics
- Child
- Copper-Transporting ATPases
- DNA -- genetics
- DNA Mutational Analysis
- Female
- Genetic Predisposition to Disease
- Genotype
- Hepatolenticular Degeneration -- diagnosis
- Humans
- Male
- Mutation
- Pedigree
- Polymerase Chain Reaction
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Publication Type: Journal Article
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