New glucose-6-phosphate dehydrogenase mutations from various ethnic groups.
Blood
; 80(1): 255-6, 1992 Jul 01.
Article
en En
| MEDLINE
| ID: mdl-1611091
ABSTRACT
Seven new mutations that produce glucose 6 phosphate dehydrogenase (G6PD) deficiency are described. Three are in variants that were biochemically characterized and described previously, while four were found in samples that had not been characterized biochemically. Several of the mutations affect the amino acids that are mutated in other G6PD variants. As had been noted previously, variants that are associated with nonspherocytic anemia are located either near the glucose 6 phosphate or the NADP binding sites. Variants more distant from these sites are not associated with chronic hemolysis.
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Banco de datos:
MEDLINE
Asunto principal:
Glucosafosfato Deshidrogenasa
/
Deficiencia de Glucosafosfato Deshidrogenasa
Límite:
Humans
País como asunto:
America do sul
/
Asia
/
Chile
/
Europa
/
Mexico
Idioma:
En
Año:
1992
Tipo del documento:
Article