Experimental generation of SNP haplotype signatures in patients with sickle cell anaemia.

<h4>Background</h4>Sickle cell anemia is caused by a single type of mutation, a homozygous A→T substitution in the ß globin gene. Clinical severity is diverse, partially due to additional, disease-modifying genetic factors. We are studying one such modifier locus, HMIP (HBS1L-MYB interge...

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Bibliographic Details
Main Authors: Stephan Menzel, Jian Qin, Nisha Vasavda, Swee Lay Thein, Ramesh Ramakrishnan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-09-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0013004&type=printable
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