Neurofilament light chain reflects motor impairment in myotonic dystrophy type 1
IntroductionMyotonic dystrophy type 1 (DM1) is a genetic disorder caused by CTG trinucleotide repeat expansion in the dystrophia myotonica-protein kinase (DMPK) gene and is characterized by progressive muscle weakness with multisystemic involvement, including the central nervous system (CNS). Neurof...
Furkejuvvon:
| Váldodahkkit: | , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Frontiers Media S.A.
2026-05-01
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| Ráidu: | Frontiers in Neurology |
| Fáttát: | |
| Liŋkkat: | https://www.frontiersin.org/articles/10.3389/fneur.2026.1820238/full |
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