about
Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species ComparisonsCalcium Dyshomeostasis in Tubular Aggregate MyopathyInborn errors of energy metabolism associated with myopathies.Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation.Tubular aggregate myopathy: a case reportEndosomal phosphoinositides and human diseases.Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2.Myofibrillar Myopathies: New Perspectives from Animal Models to Potential Therapeutic Approaches.
P921
Q26773024-60CB100A-7A9D-4B90-85FA-78EF62D885E6Q28078298-49DA3629-9C11-48BF-898E-9123DAA2D6EAQ33879587-CB9D283B-8726-4F67-878C-B2145DF3F7C0Q34461438-DB607FD1-BDDB-49B6-8740-2DE1D8771CE4Q35067335-DCF15F6C-DA57-40EE-9333-23E91D2FCEEEQ37024588-C1395ED6-5103-4BD5-BF01-951F96FDE61BQ37289753-DE9BC090-DC7E-4794-9468-B7C52D3A81F2Q38749264-78CCF47C-024B-4FF0-896C-7718897F7ADE
P921
description
human disease
@en
maladie
@fr
مرض يصيب الإنسان
@ar
name
congenital structural myopathy
@en
miopatía congénita estructural
@es
myopathie congénitale structurale
@fr
type
label
congenital structural myopathy
@en
miopatía congénita estructural
@es
myopathie congénitale structurale
@fr
altLabel
miopatia congenita estructural
@es
myopathies congénitales structurales
@fr
prefLabel
congenital structural myopathy
@en
miopatía congénita estructural
@es
myopathie congénitale structurale
@fr
P486
P1748
P1995
P279
P2892
P31
P486
P672
C05.651.575
C10.668.491.550