Intraepidermal nerve fibre density as biomarker in Charcot–Marie–Tooth disease type 1A

Charcot–Marie–Tooth disease type 1A, caused by a duplication of the gene peripheral myelin protein 22 kDa, is the most frequent subtype of hereditary peripheral neuropathy with an estimated prevalence of 1:5000. Patients suffer from sensory deficits, muscle weakness and foot deformities. There is no...

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Detalles Bibliográficos
Autores principales: Hartmannsberger, Beate, Doppler, Kathrin, Stauber, Julia, Schlotter-Weigel, Beate, Young, Peter, Sereda, Michael W, Sommer, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425304/
https://www.ncbi.nlm.nih.gov/pubmed/32954280
http://dx.doi.org/10.1093/braincomms/fcaa012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425304/
https://www.ncbi.nlm.nih.gov/pubmed/32954280
http://dx.doi.org/10.1093/braincomms/fcaa012

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