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Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?

INTRODUCTION: Charcot–Marie–Tooth neuropathy (CMT) is a genetically heterogeneous group of peripheral neuropathies. In addition to the classical clinical phenotype, additional features can occur. METHODS: We studied a wide range of additional features in a cohort of 49 genetically confirmed CMT pati...

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Detalles Bibliográficos
Autores principales:	Werheid, Friederike, Azzedine, Hamid, Zwerenz, Eva, Bozkurt, Ahmet, Moeller, Marcus J., Lin, Lilian, Mull, Michael, Häusler, Martin, Schulz, Jörg B., Weis, Joachim, Claeys, Kristl G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2016
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782242/ https://www.ncbi.nlm.nih.gov/pubmed/27088055 http://dx.doi.org/10.1002/brb3.451

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