Myopathy and parkinsonism in phosphoglycerate kinase deficiency

Author:

Sotiriou Evangelia,Greene Paul,Krishna Sindu,Hirano Michio,DiMauro Salvatore

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference15 articles.

1. PGK deficiency;Beutler;Br J Haematol,2007

2. Molecular defect of a phosphoglycerate kinase variant associated with haemolytic anaemia and neurological disorders in a large kindred;Turner;Br J Haematol,1995

3. Two new phosphoglycerate kinase mutations associated with chronic haemolytic anaemia and neurological dysfunction in two patients from Spain;Noel;Br J Haematol,2005

4. Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerations;Spiegel;Neuromuscul Disord,2009

5. Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes;Valentine;N Engl J Med,1969

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