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The molecular basis of disorders of red cell enzymes.

作者信息

McMullin M F

机构信息

Department of Haematology, Queen's University of Belfast, UK.

出版信息

J Clin Pathol. 1999 Apr;52(4):241-4. doi: 10.1136/jcp.52.4.241.

Abstract
摘要

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本文引用的文献

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Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiency.
Hum Mutat. 1997;10(4):290-4. doi: 10.1002/(SICI)1098-1004(1997)10:4<290::AID-HUMU4>3.0.CO;2-L.
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G6PD: population genetics and clinical manifestations.
Blood Rev. 1996 Mar;10(1):45-52. doi: 10.1016/s0268-960x(96)90019-3.
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New insights into G6PD deficiency.
Br J Haematol. 1996 Sep;94(4):585-91.
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Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
Am J Hematol. 1996 Feb;51(2):122-32. doi: 10.1002/(SICI)1096-8652(199602)51:2<122::AID-AJH5>3.0.CO;2-#.

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