Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration. [electronic resource]
Producer: 20161031Description: 18764-70 p. digitalISSN:- 1676-5680
- Adenosine Triphosphatases -- genetics
- Adolescent
- Adult
- Aged
- Alleles
- Asymptomatic Diseases
- Base Sequence
- Cation Transport Proteins -- genetics
- Child
- Child, Preschool
- Chorionic Villi Sampling
- Copper-Transporting ATPases
- Exons
- Female
- Fetus
- Gene Expression
- Gene Frequency
- Haplotypes
- Hepatolenticular Degeneration -- diagnosis
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Pedigree
- Polymorphism, Genetic
- Pregnancy
- Prenatal Diagnosis -- methods
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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