Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia-Reference-Cited by-同舟云学术

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

Published:1998-06 Issue:4 Volume:101 Page:670-675
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:British Journal of Haematology

Author:

Vulliamy Tom J.¹,Kaeda Jaspal S.¹,Ait‐Chafa Dahlila¹,Mangerini Rosa²,Roper David¹,Barbot Jose³,Mehta Athul B.⁴,Athanassiou‐Metaxa ⁵,Luzzatto Lucio⁶,Mason Philip J.¹

Affiliation:

1. Department of Haematology, Imperial College School of Medicine, Hammersmith Hospital, London, U.K.,

2. Dipartimento di Oncologia Clinica e Sperimentale, Universitá di Genova and Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy,

3. Minesterio da Saude, Hospital Central Especializado de Criancas Maria Pia, Porto, Portugal,

4. Department of Haematology, Royal Free Hospital, London, U.K.,

5. First Paediatric Clinic, University of Thessaloniki, Greece,

6. Department of Human Genetics, Memorial Sloan‐Kettering Cancer Center, New York, U.S.A.

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2141.1998.00763.x

Reference26 articles.

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2. G-6-PD Walter Reed: Possible insight into “structural” NADP in G-6-PD

3. G6PD: Population genetics and clinical manifestations

4. DNA‐sequence abnormalities of human glucose‐6‐phosphate‐dehydrogenase variants;Beutler E.;Journal of Biological Chemistry,1991

5. New glucose‐6‐phosphate dehydrogenase mutations from various ethnic groups;Beutler E.;Blood,1992

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