| Literature DB >> 9494043 |
P J Hutt1, A V Pisciotta, V F Fairbanks, S N Thibodeau, M M Green.
Abstract
Among the causes of congenital methemoglobinemia, Hb M-Milwaukee-2 was one of the earliest described, in a patient who also had Hb E trait. The structure of Hb M-Milwaukee-2 has been elusive. DNA sequence analysis, as here reported, proves that this hemoglobin variant is due to the mutation CAC-->TAC at codon 92 of the beta-globin gene, corresponding to the substitution of tyrosine for histidine. This mutation is identical with that presumed to be the cause of Hb M-Hyde Park and Hb M-Akita. In addition, the DNA mutation of Hb E, GAG-->AAG at codon 26, was confirmed in this case.Entities:
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Year: 1998 PMID: 9494043 DOI: 10.3109/03630269809071512
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849