Haptoglobin Gene Polymorphisms in Sickle Cell Disease Patients with Different β<sup>S</sup>-Globin Gene Haplotypes
Author(s) -
Adekunle Adekile,
M.Z. Haider
Publication year - 2010
Publication title -
medical principles and practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.426
H-Index - 45
eISSN - 1423-0151
pISSN - 1011-7571
DOI - 10.1159/000320302
Subject(s) - genotyping , haptoglobin , allele , medicine , haplotype , genotype , allele frequency , disease , immunology , gene , gastroenterology , genetics , biology
To investigate the prevalence of haptoglobin (Hp) gene alleles in Kuwaiti sickle cell disease (SCD) patients, who generally have a mild phenotype, and compare the pattern to Nigerian SCD patients whose SCD phenotype is more severe.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom