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EMILIN1 gene variant associated with polyneuropathy, language impairment, and motor dysfunction.
Palumbo, Francesca; Moglia, Cristina; Romano, Alessandro; Tessa, Alessandra; Canosa, Antonio; Calvo, Andrea; Gallone, Salvatore.
Afiliación
  • Palumbo F; Department of Neuroscience, University of Turin, ALS Centre, Turin, Italy.
  • Moglia C; Department of Neuroscience, University of Turin, ALS Centre, Turin, Italy.
  • Romano A; SC Neurologia 1U, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
  • Tessa A; Experimental Neuropathology Unit, Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Canosa A; Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Stella Maris Foundation, Pisa, Italy.
  • Calvo A; Department of Neuroscience, University of Turin, ALS Centre, Turin, Italy.
  • Gallone S; SC Neurologia 1U, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
Am J Med Genet A ; 194(11): e63808, 2024 Nov.
Article en En | MEDLINE | ID: mdl-38963291
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Polineuropatías Idioma: En Revista: Am J Med Genet A / Am. j. med. genet., Part A / American journal of medical genetics. Part A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Polineuropatías Idioma: En Revista: Am J Med Genet A / Am. j. med. genet., Part A / American journal of medical genetics. Part A Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article