Molecular Analysis of the Rare In(Lu) Blood Type: Toward Decoding the Phenotypic Outcome of Haploinsufficiency for the Transcription Factor KLF1
Author:
Affiliation:
1. National Institute of Blood Transfusion (INTS); Paris; France
2. Laboratoire de Biochimie et Génétique; CHU Hôpital Henri Mondor; Créteil; France
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22218/fullpdf
Reference30 articles.
1. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia;Arnaud;Am J Hum Genet,2010
2. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin;Borg;Nat Genet,2010
3. A serological and genetical study of multiple antibodies formed in response to blood transfusion by a patient with lupus erythematosus diffusus;Callender;Ann Eugen,1946
4. The expected blood-group antibody, anti-Lub;Chanarin;Nature,1956
5. The molecular basis of HPFH in a British family identified by heteroduplex formation;Craig;Br J Haematol,1993
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