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Mitochondrial Mutations Can Alter Neuromuscular Transmission in Congenital Myasthenic Syndrome and Mitochondrial Disease.
O'Connor, Kaela; Spendiff, Sally; Lochmüller, Hanns; Horvath, Rita.
Affiliation
  • O'Connor K; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada.
  • Spendiff S; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.
  • Lochmüller H; Centre for Neuromuscular Disease, University of Ottawa Brain and Mind Research Institute, Ottawa, ON K1H 8M5, Canada.
  • Horvath R; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada.
Int J Mol Sci ; 24(10)2023 May 09.
Article in En | MEDLINE | ID: mdl-37239850
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myasthenic Syndromes, Congenital / Mitochondrial Diseases / Organic Anion Transporters Limits: Humans Language: En Journal: Int J Mol Sci Year: 2023 Type: Article Affiliation country: Canada
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myasthenic Syndromes, Congenital / Mitochondrial Diseases / Organic Anion Transporters Limits: Humans Language: En Journal: Int J Mol Sci Year: 2023 Type: Article Affiliation country: Canada