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

Internet

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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