ATP7B is a copper transporting P-type ATPase defective in the autosomal recessive copper storage disorder, Wilson disease (WND). Functional assessment of variants helps to distinguish normal from disease-causing variants and provides information on important amino acid residues. A total of 11 missen
A model of the monosaccharide uphill transporting cell membrane system in yeast
✍ Scribed by Milan Höfer
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- English
- Weight
- 230 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-5193
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