Second report of Hb toulon [α77(EF6)pro→his] in a Canadian family of Italian descent

Hemoglobin

Volumn 24, Issue 4, 2000, Pages 359-360

  Waye, J S ^a   Eng, B ^a   Chui, D H K ^a   Powers, P J ^a   Lafferty, J D ^a  

^a MCMASTER UNIVERSITY MEDICAL CENTRE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN A2; HEMOGLOBIN TOULON; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; ELECTROPHORESIS; GENE AMPLIFICATION; GENE SEQUENCE; HEMOGLOBIN ANALYSIS; HEMOGLOBIN DETERMINATION; HUMAN; HUMAN CELL; ISOELECTRIC FOCUSING; MALE; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS;

EID: 0033677748     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630260008993146     Document Type: Article

References (5)

1. A Syllabus of Human Hemoglobin Variants (1996)
2. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
3. Locus assignment of human α-globin mutations by selective amplification and direct sequencing
4. DNA sequencing with chain termination inhibitors
5. Hb Toulon [α77(EF6)Pro→His]: A new variant due to a mutation in the α2 gene found during measurement of glycated hemoglobin