Argininemia is a rare autossomal recessive disorder caused by deficiency in the cytosolic liver-type arginase enzyme (L-arginine urea-hydrolase; E.C. 3.5.3.1). In order to investigate the molecular basis for argininemia in four unrelated Portuguese patients (two from northern Portugal and two from M
โฆ LIBER โฆ
Five Novel Mutations in ARG1 Gene in Chinese Patients of Argininemia
โ Scribed by Wu, Tong-Fei; Liu, Yu-Peng; Li, Xi-Yuan; Wang, Qiao; Ding, Yuan; Ma, Yan-Yan; Song, Jin-Qing; Yang, Yan-Ling
- Book ID
- 123604952
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 183 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0887-8994
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