Your browser doesn't support javascript.
loading
A Novel CCT5 Missense Variant Associated with Early Onset Motor Neuropathy.
Antona, Vincenzo; Scalia, Federica; Giorgio, Elisa; Radio, Francesca C; Brusco, Alfredo; Oliveri, Massimiliano; Corsello, Giovanni; Lo Celso, Fabrizio; Vadalà, Maria; Conway de Macario, Everly; Macario, Alberto J L; Cappello, Francesco; Giuffrè, Mario.
Afiliação
  • Antona V; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, 90127 Palermo, Italy.
  • Scalia F; Department of Biomedicine, Neuroscience and Advanced Diagnostics (BIND), University of Palermo, 90127 Palermo, Italy.
  • Giorgio E; Department of Biomolecular Strategies, Genetics and Advanced Therapies, Euro-Mediterranean Institute of Science and Technology (IEMEST), 90139 Palermo, Italy.
  • Radio FC; Department of Medical Sciences, University of Torino, 10126 Torino, Italy.
  • Brusco A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù IRCSS, 00146 Rome, Italy.
  • Oliveri M; Department of Medical Sciences, University of Torino, 10126 Torino, Italy.
  • Corsello G; Department of Psychological, Pedagogical and Educational Sciences, University of Palermo, 90128 Palermo, Italy.
  • Lo Celso F; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, 90127 Palermo, Italy.
  • Vadalà M; Department of Physics and Chemistry-Emilio Segrè, University of Palermo, 90128 Palermo, Italy.
  • Conway de Macario E; Ionic Liquids Laboratory, Institute of Structure of Matter, Italian National Research Council (ISM-CNR), 00133 Rome, Italy.
  • Macario AJL; Department of Biomedicine, Neuroscience and Advanced Diagnostics (BIND), University of Palermo, 90127 Palermo, Italy.
  • Cappello F; Department of Biomolecular Strategies, Genetics and Advanced Therapies, Euro-Mediterranean Institute of Science and Technology (IEMEST), 90139 Palermo, Italy.
  • Giuffrè M; Department of Microbiology and Immunology, School of Medicine, University of Maryland at Baltimore-Institute of Marine and Environmental Technology (IMET), Baltimore, MD 21202, USA.
Int J Mol Sci ; 21(20)2020 Oct 15.
Article em En | MEDLINE | ID: mdl-33076433
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatia Hereditária Motora e Sensorial / Mutação de Sentido Incorreto / Chaperonina com TCP-1 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Newborn Idioma: En Revista: Int J Mol Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuropatia Hereditária Motora e Sensorial / Mutação de Sentido Incorreto / Chaperonina com TCP-1 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Newborn Idioma: En Revista: Int J Mol Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália