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Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern.Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?The relative frequency of common neuromuscular diagnoses in a reference center.Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers.Muscle Biopsy ReportingCentral core myopathy with autophagyClinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophyLimb Length Discrepancy on an 11-Month-Old Boy with Osteoid OsteomaLMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability
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Q35315272-78339FC8-874B-40A5-B053-3734308EBC18Q38253968-286A3BBC-B855-42FB-A88E-71A301646A88Q47681679-96FB3F8C-54E3-48E7-A512-A72E09550B42Q47865157-D2DDC42D-4119-4469-9D70-49B11FB84B57Q88230709-14FAC163-D2C2-458C-AC3D-7DE94EE02FA7Q89210084-5AEE68C1-3850-41E0-B70D-C1D307FB64BEQ91578154-08A23F54-C019-4B89-95E0-1570A23D16AAQ92297606-78748126-0ADD-4667-8DB3-7251AED8B314Q92607757-F107BA81-EA0E-4B03-8DCE-3648D7FD2EA6
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Ana Cotta
@en
Ana Cotta
@nl
type
label
Ana Cotta
@en
Ana Cotta
@nl
prefLabel
Ana Cotta
@en
Ana Cotta
@nl
P31
P496
0000-0003-2931-6589