Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years

Charcot–Marie–Tooth (CMT) disease is the most commonly inherited neurological disorder. This study includes patients affected by CMT during regular follow-ups at the CMT clinic in Genova, a neuromuscular university center in the northwest of Italy, with the aim of describing the genetic distribution...

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Detalles Bibliográficos
Autores principales: Gemelli, Chiara, Geroldi, Alessandro, Massucco, Sara, Trevisan, Lucia, Callegari, Ilaria, Marinelli, Lucio, Ursino, Giulia, Hamedani, Mehrnaz, Mennella, Giulia, Stara, Silvia, Maggi, Giovanni, Mori, Laura, Schenone, Cristina, Gotta, Fabio, Patrone, Serena, Mammi, Alessia, Origone, Paola, Prada, Valeria, Nobbio, Lucilla, Mandich, Paola, Schenone, Angelo, Bellone, Emilia, Grandis, Marina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8948690/
https://www.ncbi.nlm.nih.gov/pubmed/35330153
http://dx.doi.org/10.3390/life12030402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8948690/
https://www.ncbi.nlm.nih.gov/pubmed/35330153
http://dx.doi.org/10.3390/life12030402

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