Identification of Candidate Protein Markers in Skeletal Muscle of Laminin-211-Deficient CMD Type 1A-Patients

Laminin-211 deficiency leads to the most common form of congenital muscular dystrophy in childhood, MDC1A. The clinical picture is characterized by severe muscle weakness, brain abnormalities and delayed motor milestones defining MDC1A as one of the most severe forms of congenital muscular diseases....

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Detalles Bibliográficos
Autores principales: Kölbel, Heike, Hathazi, Denisa, Jennings, Matthew, Horvath, Rita, Roos, Andreas, Schara, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514157/
https://www.ncbi.nlm.nih.gov/pubmed/31133972
http://dx.doi.org/10.3389/fneur.2019.00470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514157/
https://www.ncbi.nlm.nih.gov/pubmed/31133972
http://dx.doi.org/10.3389/fneur.2019.00470

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