Two new mutations of the glucose-6-phosphate dehydrogenase (G6PD) gene associated with haemolytic anaemia: Clinical, biochemical and molecular relationships

British Journal of Haematology

Volumn 98, Issue 3, 1997, Pages 578-582

  Zarza, R ^a   Pujades, A ^a   Rovira, A ^a   Saavedra, R ^b   Fernandez, J ^a   Aymerich, M ^a   Vives Corrons, J Ll ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b HOSPITAL UNIVERSITARIO DE GUADALAJARA   (Spain)

Author keywords

Chronic nonspherocytic haemolytic anaemia; Favism; G6PD deficiency; G6PD Madrid; G6PD Valladolid

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ARTICLE; CASE REPORT; ENZYME ANALYSIS; EXON; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYSIS; HEMOLYTIC ANEMIA; HUMAN; MALE; NUCLEIC ACID BASE SUBSTITUTION; POINT MUTATION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0030964595     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1997.2563071.x     Document Type: Article

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