Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia-Reference-Cited by-同舟云学术

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Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia

Published:1977-10 Issue:5 Volume:7 Page:427-435
ISSN:0014-2972
Container-title:European Journal of Clinical Investigation
language:en
Short-container-title:Eur J Clin Invest

Author:

KRIETSCH WOLFGANG K. G.,KRIETSCH HELGARD,KAISER WOLFRAM,DUNNWALD MANFRED,KUNTZ GÜNTER W. K.,DUHM† JOCHEN,BÜCHER THEODOR

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.1977.tb01630.x/fullpdf

Reference42 articles.

1. Distribution of genetic variants of erythrocyte phosphoglycerate kinase (PGK) and phosphohexose isomerase (PHI) among some population groups in south-east Asia and Oceania

2. Electrophoresis of phosphoglycerate kinase

3. The Distribution of Blood, Serum Protein and Enzyme Groups on Manus Island (Admiralty Islands, New Guinea)

Cited by 45 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population;Genes;2019-10-10

2. A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: Molecular and functional characterization;Molecular Genetics and Metabolism;2012-08

3. Enzymatic and metabolic characterization of the phosphoglycerate kinase deficiency associated with chronic hemolytic anemia caused by the PGK-Barcelona mutation;Blood Cells, Molecules, and Diseases;2011-03

4. PGK deficiency;British Journal of Haematology;2007-01

5. The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA;British Journal of Haematology;2006-07

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