Rh null is a rare autosomal recessive disorder characterized by an absence of Rh antigens and a varying degree of hemolytic anemia and spherostomatocytosis. We report studies of two Japanese Rh null cases and describe three new missense mutations of RHAG, the locus that encodes Rh50 glycoprotein and
β¦ LIBER β¦
Rhnull syndrome: identification of a novel mutation in RHce
β Scribed by K.A. Rosa; M.E. Reid; C. Lomas-Francis; V.I. Powell; F.F. Costa; S.T. Stinghen; A.M. Watanabe; E.K. Carboni; J.P. Baldon; M.M.F. Jucksch; L. Castilho
- Book ID
- 109142895
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 94 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0372-1248
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