Shedding light on motor premanifest myotonic dystrophy type 1: A molecular, muscular and central nervous system follow‐up study

BACKGROUND AND PURPOSE: Myotonic dystrophy type 1 (DM1) is a hereditary and multisystemic disease that is characterized by heterogeneous manifestations. Although muscular impairment is central to DM1, a premanifest DM1 form has been proposed for those characterized by the absence of muscle signs in...

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Detalles Bibliográficos
Autores principales: Garmendia, Joana, Labayru, Garazi, Zulaica, Miren, Villanúa, Jorge, López de Munain, Adolfo, Sistiaga, Andone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Muscle and NMJ disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092190/
https://www.ncbi.nlm.nih.gov/pubmed/36256504
http://dx.doi.org/10.1111/ene.15604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092190/
https://www.ncbi.nlm.nih.gov/pubmed/36256504
http://dx.doi.org/10.1111/ene.15604

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