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Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell JJ, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Suliman A, Patra PK, Milton JN, Farrer LA, Chui DH, Al-Ali AK, Sebastiani P, Steinberg MH. Vathipadiekal V, et al. Among authors: steinberg mh. Am J Hematol. 2016 Jun;91(6):E308-11. doi: 10.1002/ajh.24368. Epub 2016 Apr 28. Am J Hematol. 2016. PMID: 27185208 Free PMC article. No abstract available.
A novel sickle hemoglobin: hemoglobin S-south end.
Luo HY, Adewoye AH, Eung SH, Skelton TP, Quillen K, McMahon L, Steinberg MH, Chui DH. Luo HY, et al. Among authors: steinberg mh. J Pediatr Hematol Oncol. 2004 Nov;26(11):773-6. doi: 10.1097/00043426-200411000-00019. J Pediatr Hematol Oncol. 2004. PMID: 15543018
360 results