Candidate imaging biomarkers for PMP22 ‐related inherited neuropathies

OBJECTIVE: Charcot–Marie–Tooth type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsy (HNPP) are caused by mutations to the peripheral myelin protein 22 (PMP22) gene. A need exists for sensitive and reliable biomarkers of progression and treatment response. Magnetic resonance ima...

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Detalles Bibliográficos
Autores principales: Roth, Alison R., Li, Jun, Dortch, Richard D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268861/
https://www.ncbi.nlm.nih.gov/pubmed/35656877
http://dx.doi.org/10.1002/acn3.51561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268861/
https://www.ncbi.nlm.nih.gov/pubmed/35656877
http://dx.doi.org/10.1002/acn3.51561

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