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
โฆ LIBER โฆ
Rhmod Syndrome: A Family Study of the Translation-Initiator Mutation in the Rh50 Glycoprotein Gene
โ Scribed by C.-H. Huang; G.-J. Cheng; M.E. Reid; Y. Chen
- Book ID
- 117852687
- Publisher
- American Society of Human Genetics
- Year
- 1999
- Tongue
- English
- Weight
- 842 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/302215
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