Mutation in GNE Downregulates Peroxiredoxin IV Altering ER Redox Homeostasis

Chanana, P; Padhy, G; Bhargava, K; Arya, R

Arya, R (reprint author), Jawaharlal Nehru Univ, Sch Biotechnol, New Delhi 110067, India.

NEUROMOLECULAR MEDICINE, 2017; 19 (4): 525

Abstract

GNE myopathy is a rare neuromuscular genetic disorder characterized by early adult onset and muscle weakness due to mutation in sialic acid biosynthet......

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