Your browser doesn't support javascript.
loading
Differential Domain Distribution of gnomAD- and Disease-Linked Connexin Missense Variants.
Bai, Donglin; Wang, Jiayi; Li, Tianhe; Chan, Ryan; Atalla, Mena; Chen, Robert C; Khazaneh, Mohammad T; An, Raphael J; Stathopulos, Peter B.
Affiliation
  • Bai D; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Wang J; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Li T; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Chan R; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Atalla M; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Chen RC; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Khazaneh MT; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • An RJ; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
  • Stathopulos PB; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.
Int J Mol Sci ; 22(15)2021 Jul 22.
Article in En | MEDLINE | ID: mdl-34360596

Full text: 1 Database: MEDLINE Main subject: Gap Junctions / Connexins / Mutation, Missense / Databases, Genetic / Genetics, Population / Genetic Diseases, Inborn Limits: Humans Language: En Journal: Int J Mol Sci Year: 2021 Type: Article Affiliation country: Canada

Full text: 1 Database: MEDLINE Main subject: Gap Junctions / Connexins / Mutation, Missense / Databases, Genetic / Genetics, Population / Genetic Diseases, Inborn Limits: Humans Language: En Journal: Int J Mol Sci Year: 2021 Type: Article Affiliation country: Canada