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Pyrimidine-5′-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5′-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression
✍ Scribed by dos Santos, Andrey; Dantas, Larissa Elizabeth Cordeiro; Traina, Fabiola; de Albuquerque, Dulcineia Martins; Chaim, Elinton Adami; Olalla Saad, Sara T.
- Book ID
- 126761184
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 975 KB
- Volume
- 53
- Category
- Article
- ISSN
- 1079-9796
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