A new AQP1 null allele identified in a Gypsy woman who developed an anti-CO3 during her first pregnancy
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1423-0410.2012.01590.x/fullpdf
Reference19 articles.
1. Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels;Preston;Science,1994
2. A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system;Arnaud;Transfusion,2010
3. A single mutation inside the NPA motif of aquaporin-1 found in a Colton-null phenotype;Chrétien;Blood,1999
4. An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN;Joshi;Transfusion,2001
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1. ABCB6, an ABC Transporter Impacting Drug Response and Disease;The AAPS Journal;2017-11-30
2. The AQP1 de1601G mutation in different European Romani (Gypsy) populations;BLOOD TRANSFUS-ITALY;2016
3. Role of the N-terminal transmembrane domain in the endo-lysosomal targeting and function of the human ABCB6 protein;Biochemical Journal;2015-03-20
4. The AQP1 mutation c.601deIG causes the Co-negative phenotype in four patients belonging to the Romani (Gypsy) ethnic group;BLOOD TRANSFUS-ITALY;2014
5. Energetic and Molecular Water Permeation Mechanisms of the Human Red Blood Cell Urea Transporter B;PLoS ONE;2013-12-20
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