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Prevalence, pathological mechanisms, and genetic basis of limb-girdle muscular dystrophies: A review
Fecha de emisión
2019
Autor(es)
DOI
10.1002/jcp.27907
Temas
autosomal disorders
dystrophin
limb-girdle muscular ...
pathophysiology
weakness
dystrophin
glycoprotein
clinical feature
disease classificatio...
disease course
genetic analysis
glycosylation
human
limb girdle muscular ...
pathogenesis
prevalence
priority journal
Review
sarcomere
signal transduction
cachexia
genetics
high throughput seque...
limb girdle muscular ...
metabolism
neuromuscular disease...
pathology
skeletal muscle
Cachexia
High-Throughput Nucle...
Humans
Muscle, Skeletal
Muscular Dystrophies,...
Neuromuscular Disease...
Sarcomeres
Archivo(s)