Mutations in MYO9B are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy

BACKGROUND AND PURPOSE: Charcot–Marie–Tooth disease (CMT) is a heterogeneous group of disorders caused by mutations in at least 100 genes. However, approximately 60% of cases with axonal neuropathies (CMT2) still remain without a genetic diagnosis. We aimed at identifying novel disease genes respons...

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Detalles Bibliográficos
Autores principales: Cipriani, Silvia, Guerrero‐Valero, Marta, Tozza, Stefano, Zhao, Edward, Vollmer, Veith, Beijer, Danique, Danzi, Matt, Rivellini, Cristina, Lazarevic, Dejan, Pipitone, Giovanni Battista, Grosz, Bianca Rose, Lamperti, Costanza, Marzoli, Stefania Bianchi, Carrera, Paola, Devoto, Marcella, Pisciotta, Chiara, Pareyson, Davide, Kennerson, Marina, Previtali, Stefano C., Zuchner, Stephan, Scherer, Steven S., Manganelli, Fiore, Bähler, Martin, Bolino, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Neuropathies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099703/
https://www.ncbi.nlm.nih.gov/pubmed/36260368
http://dx.doi.org/10.1111/ene.15601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099703/
https://www.ncbi.nlm.nih.gov/pubmed/36260368
http://dx.doi.org/10.1111/ene.15601

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