An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1537-2995.2001.41101273.x/fullpdf
Reference39 articles.
1. 1. H Schenkel-Brunner , ed. Human blood groups . 2nd ed . Vienna: Springer, 2000 : 582 -6 .
2. Mutations in aquaporin-1 in Phenotypically Normal Humans Without Functional CHIP Water Channels
3. A Single Mutation Inside the NPA Motif of Aquaporin-1 Found in a Colton-Null Phenotype
4. Studies on the blood of a Co (a-b-) proposita and her family
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2. The AQP1 mutation c.601deIG causes the Co-negative phenotype in four patients belonging to the Romani (Gypsy) ethnic group;BLOOD TRANSFUS-ITALY;2014
3. Other Red Cell Antigens;Mollison's Blood Transfusion in Clinical Medicine;2013-11-30
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5. A new AQP1 null allele identified in a Gypsy woman who developed an anti-CO3 during her first pregnancy;Vox Sanguinis;2012-02-20
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