尿苷单磷酸激酶：一种具有潜在临床意义的新基因多态性。 - Suppr

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超能文献

Uridine monophosphate kinase: A new genetic polymorphism with possible clinical implications.

作者信息

Giblett E R, Anderson J E, Chen S H, Teng Y S, Cohen F

出版信息

Am J Hum Genet. 1974 Sep;26(5):627-35.

PMID:4138532

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1762733/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cb9/1762733/74d17813ae49/ajhg00444-0097-a.jpg

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本文引用的文献

QUANTITATIVE DIFFERENCES AND GENE DOSAGE IN THE HUMAN RED CELL ACID PHOSPHATASE POLYMORPHISM.人类红细胞酸性磷酸酶多态性中的定量差异与基因剂量

Nature. 1964 Jan 18;201:299-300. doi: 10.1038/201299a0.

Improved method for measuring galactose-I-phosphate uridyl transferase activity of erythrocytes.测定红细胞半乳糖-1-磷酸尿苷酰转移酶活性的改进方法。

Clin Chim Acta. 1966 Mar;13(3):369-79. doi: 10.1016/0009-8981(66)90217-8.

Genetically determined variation of adenylate kinase in man.人类中腺苷酸激酶的基因决定变异。

Nature. 1966 Jan 15;209(5020):261-3. doi: 10.1038/209261a0.

Metabolism of deoxyribonucleotides. I. Purification and properties of deoxycytidine monophosphokinase of calf thymus.

J Biol Chem. 1966 Feb 25;241(4):961-9.

Phosphoglycerate kinase: an X-linked polymorphism in man.磷酸甘油酸激酶：人类中的一种X连锁多态性。

Am J Hum Genet. 1971 Jan;23(1):87-91.

[A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency].[一种新的红细胞酶病：先天性非球形细胞溶血性贫血与遗传性红细胞腺苷酸激酶缺乏症]

Presse Med (1893). 1971 Jan 30;79(6):215-8.

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