Triose phosphate isomerase deficiency.

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作者信息

Skala H, Dreyfus J C, Vives-Corrons J L, Matsumoto F, Beutler E

出版信息

Biochem Med. 1977 Oct;18(2):226-34. doi: 10.1016/0006-2944(77)90094-1.

DOI:10.1016/0006-2944(77)90094-1

PMID:907660

Abstract

摘要

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Triose phosphate isomerase deficiency.

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引用本文的文献

Human triosephosphate isomerase deficiency resulting from mutation of Phe-240.由苯丙氨酸-240突变导致的人类磷酸丙糖异构酶缺乏症。

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Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms.遗传性磷酸丙糖异构酶（TPI）缺乏症：两名严重受影响的兄弟，其中一名有神经症状，另一名没有。

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Origin of the triosephosphate isomerase isozymes in humans: genetic evidence for the expression of a single structural locus.人类磷酸丙糖异构酶同工酶的起源：单一结构基因座表达的遗传学证据。

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Characterization of two new electrophoretic variants of human triosephosphate isomerase: stability, kinetic, and immunological properties.人磷酸丙糖异构酶两种新电泳变体的特性：稳定性、动力学及免疫学性质

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Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain.

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