Glucose-6-phosphate dehydrogenase de-
ficiency serves as a prototype of the
many human enzyme deficiencies that
are now known. Since its discovery more
than 50 years ago, the high prevalence of
the defect and the easy accessibility of
the cells that manifest it have made it a
favorite tool of biochemists, epidemiologists,
geneticists, and molecular biologists
as well as clinicians. In this brief
historical review, we trace the discovery
of this defect, its clinical manifestations,
detection, population genetics, and molecular
biology
Glucose-6-phosphate dehydrogenase de-ficiency serves as a prototype of themany human enzyme deficiencies thatare now known. Since its discovery morethan 50 years ago, the high prevalence ofthe defect and the easy accessibility ofthe cells that manifest it have made it afavorite tool of biochemists, epidemiologists,geneticists, and molecular biologistsas well as clinicians. In this briefhistorical review, we trace the discoveryof this defect, its clinical manifestations,detection, population genetics, and molecularbiology
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