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Hemoglobin ; 6(4): 391-6, 1982.
Article in English | MEDLINE | ID: mdl-7141875

ABSTRACT

An uncommon abnormal hemoglobin, Hb Belfast (beta 15 Trp replaced by Arg) was discovered in a patient of Italian origin. The patient was a 42-year-old man who developed two episodes of jaundice after a prolonged administration of an antituberculous drugs. Family studies revealed that several members were asymptomatic carriers of Hb Belfast.


Subject(s)
Hemoglobins, Abnormal/isolation & purification , Adult , Arginine , Chemical Phenomena , Chemistry , Female , Hemoglobins/analysis , Hemoglobins, Abnormal/genetics , Humans , Italy , Male , Pedigree , Tryptophan
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