NDLI: Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.

Content Provider	Semantic Scholar
Author	Amid, Ali Cheong, Melina Hanna, Meredith Hohenadel, Betty-Ann Nakamura, Lisa M. Walker, Lynda L. Odame, Isaac Kirby-Allen, Melanie Waye, John S.
Copyright Year	2015
Abstract	Sickle cell disease (SCD) is one of the most common genetic disorders worldwide and is associated with episodes of acute pain and progressive multi-organ damage.[1][1] The most common cause of SCD is homozygosity for the hemoglobin sickle (Hb S) mutation, with a minority of cases due to compound
Starting Page	115
Ending Page	119
Page Count	5
File Format	PDF HTM / HTML
DOI	10.3324/haematol.2014.117408
PubMed reference number	25682598
Journal	Medline
Volume Number	100
Issue Number	5
Alternate Webpage(s)	http://www.haematologica.org/content/haematol/100/5/e166.full.pdf
Alternate Webpage(s)	https://doi.org/10.3324/haematol.2014.117408
Journal	Haematologica
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.