Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia

British Journal of Haematology

Volumn 101, Issue 4, 1998, Pages 670-675

  Vulliamy, Tom J ^a   Kaeda, Jaspal S ^a   Ait Chafa, Dahlila ^a   Mangerini, Rosa ^b   Roper, David ^a   Barbot, Jose ^c   Mehta, Athul B ^d   Athanassiou Metaxa, M ^e   Luzzato, Lucio ^f   Mason, Philip J ^a  

^a IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

^b UNIVERSITY OF GENOA   (Italy)

^c Hosp Ctrl Especializado C   (Portugal)

^d ROYAL FREE HOSPITAL   (United Kingdom)

^e ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

^f MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

Author keywords

G6PD deficiency; G6PD Serres; Recurrent mutation

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; GENE DELETION; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYTIC ANEMIA; HUMAN; MALE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; RECURRENT DISEASE;

ADOLESCENT; ANEMIA, HEMOLYTIC; CHILD; CHILD, PRESCHOOL; CHRONIC DISEASE; GENE DELETION; GLUCOSEPHOSPHATE DEHYDROGENASE; GLYCOGEN STORAGE DISEASE TYPE I; HUMANS; INFANT, NEWBORN; MALE; MIDDLE AGED; MUTATION; POINT MUTATION;

EID: 7144257850     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1998.00763.x     Document Type: Article

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