Associated Papers
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.
Sarparanta J et al.
International Journal of Molecular Sciences, 2020
Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities.
Santos R et al.
Antioxidants & Redox Signaling, 2010
Glucose-6-phosphate dehydrogenase deficiency: a historical perspective.
Beutler E
Blood, 2008
Molecular characterization of G6PD Insuli--a novel 989 CGC --> CAC (330 Arg --> His) mutation in the Indian population.
Sukumar S et al.
Blood Cells, Molecules & Diseases, 0
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