Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases

BACKGROUND: The elucidation of pathomechanisms leading to the manifestation of rare (genetically caused) neurological diseases including neuromuscular diseases (NMD) represents an important step toward the understanding of the genesis of the respective disease and might help to define starting point...

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Detalles Bibliográficos
Autores principales: Hentschel, Andreas, Czech, Artur, Münchberg, Ute, Freier, Erik, Schara-Schmidt, Ulrike, Sickmann, Albert, Reimann, Jens, Roos, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874489/
https://www.ncbi.nlm.nih.gov/pubmed/33563298
http://dx.doi.org/10.1186/s13023-020-01669-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874489/
https://www.ncbi.nlm.nih.gov/pubmed/33563298
http://dx.doi.org/10.1186/s13023-020-01669-1

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