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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Bibliographic Details
Published in:Front Neurol
Main Authors: Kölbel, Heike, Hathazi, Denisa, Jennings, Matthew, Horvath, Rita, Roos, Andreas, Schara, Ulrike
Format: Artigo
Language:Inglês
Published: Frontiers Media S.A. 2019
Subjects:
Neurology
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6514157/
https://ncbi.nlm.nih.gov/pubmed/31133972
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.00470
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