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pro vyhledávání: '"Lucila De León"'
Autor:
Mariana Martínez Barreiro, Lucia Vázquez Alberdi, Lucila De León, Guadalupe Avellanal, Andrea Duarte, Maximiliano Anzibar Fialho, Jérôme Baranger, Miguel Calero, Nicolás Rubido, Mickael Tanter, Carlos Negreira, Javier Brum, Juan Pablo Damián, Alejandra Kun
Publikováno v:
Biology, Vol 12, Iss 10, p 1324 (2023)
The main human hereditary peripheral neuropathy (Charcot-Marie-Tooth, CMT), manifests in progressive sensory and motor deficits. Mutations in the compact myelin protein gene pmp22 cause more than 50% of all CMTs. CMT1E is a subtype of CMT1 myelinopat
Externí odkaz:
https://doaj.org/article/646ddf5f16ca456891999fd89466cc07
