Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1468-1331.2000.00012.x/fullpdf
Reference7 articles.
1. Phosphoglycerate kinase deficiency: a new cause of recurrent myoglobinuria.;DiMauro;Trans Am Neurol Soc,1981
2. Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia.;Kraus;Biochem Biophys Res Commun,1968
3. Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia.;Krietsch;Eur J Clin Invest,1977
4. A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking haemolytic anaemia.;Rosa;Blood,1982
5. Phosphoglycerate kinase deficiency.;Sugie;Neurol,1994
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