Hemoglobin · 1992 · 10 citations · 20 references
Life SciencesGeneticsMolecular GeneticsBiochemical GeneticsHuman GeneticsMedical GeneticsAnemiaGenetic DisordersHaplotype AnalysisHematologic DisordersRed Blood Cell DisordersSickle Cell DiseaseHemoglobin DysfunctionMolecular Diagnosis Of HemoglobinopathiesReplacementSickle Cell Anemia
The silent Hb Muscat with a Leu----Val replacement at position beta 32 was discovered by reversed phase high performance liquid chromatography in two members of an Arabian family from Oman; in one person Hb Muscat occurred with Hb S and in the other with Hb A. Hb Muscat is slightly unstable but its presence has no apparent adverse effect on the health of its carriers. Additional hemoglobin abnormalities observed in this family were a common alpha-thalassemia-2 (-3.7 kb) and Hb S. The beta S haplotypes in the heterozygous carriers and the two sickle cell anemia patients were #19 (Benin) and #20 (Bantu); the latter likely originated from an East African population.
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J. B. Clegg, Michael A. Naughton, D. J. Weatherall · Journal of Molecular Biology · 1966 · 1.5K citations
The Hemoglobinopathies. Techniques of Identification.
Annals of Internal Medicine · 1978 · 360 citations