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This is likely to be important in diseases beyond type 2 diabetes where metformin is used chronically
Mutations of this gene were found in 11% of patients with autosomal recessive peripheral neuropathy, and in 76% of patients with axonal neuropathy plus neuromyotonia (92
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[DOI] [PubMed] [Google Scholar] 102.Wawrzczak-Bargiea A., Zikowska B., Piotrowska A., Starnowska-Sok J., Rojewska E., Mika J., Przewocka B., Przewocki R
