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Hb Tacoma: G>T or G>C, and Does It Matter?
Moore, Jordyn A; Pullon, Beverley M; Wang, Darrell; Brennan, Stephen O.
Afiliação
  • Moore JA; Specialist Biochemistry, Canterbury Health Laboratories, Christchurch, New Zealand.
  • Pullon BM; Specialist Haematology, Waikato Hospital, Hamilton, New Zealand.
  • Wang D; Molecular Pathology, Canterbury Health Laboratories, Christchurch, New Zealand.
  • Brennan SO; Molecular Pathology Laboratory, University of Otago, Christchurch, New Zealand.
Hemoglobin ; 45(3): 203-206, 2021 May.
Article em En | MEDLINE | ID: mdl-34233561
Hb Tacoma [ß30(B12)Arg→Ser] is a missense variant that is caused by either an AGG>AGT or AGG>AGC substitution at codon 30 of the HBB gene. Currently, the latter is classified as a rare cause of ß0-thalassemia (ß0-thal). We propose that HBB: c.93G>C has been incorrectly assigned as ß0-thal and discuss whether HBB: c.93G>T or HBB: c.93G>C should be classified as ß+-thal instead, or as ß-globin variants without thalassemic effect. We present several subjects who are heterozygous for Hb Tacoma, one with HBB: c.93G>T and two with HBB: c.93G>C, to support our conclusions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemoglobinas Anormais / Talassemia beta Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemoglobinas Anormais / Talassemia beta Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article