An update on the I blood group system
Author:
Publisher
Walter de Gruyter GmbH
Subject
Hematology,General Medicine,Immunology and Allergy
Link
https://www.exeley.com/exeley/journals/immunohematology/35/3/pdf/10.21307_immunohematology-2020-019.pdf
Reference46 articles.
1. International Society for Blood Transfusion. Names for I (ISBT 027) blood group alleles. www.isbtweb.org.
2. Case report of homozygous deletion involving the first coding exons of the upstream region of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract;BMC Med Genet,2016
3. Deletion at the GCNT2 locus causes autosomal recessive congenital cataracts;PLoS One,2016
4. Identification of epigenetic silencing of GCNT2 expression by comprehensive real-time PCR screening in colorectal cancer;J Clin Oncol,2014
5. A new IGNT allele found in the adult i-negative in Japanese without congenital cataracts;Vox Sang,2011
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