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Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor

✍ Scribed by M.-H. Yang; L. Li; Y.-F. Kuo; Y.-S. Hung; L.-C. Yu; C.-S. Hung; S.-J. L. Tsai; K.-S. Lin; D.-C. Chu


Book ID
110869355
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
803 KB
Volume
21
Category
Article
ISSN
0958-7578

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