Mutations in human collagen VI genes cause a spectrum of musculoskeletal conditions in children and adults collectively termed collagen VI-related myopathies (COL6-RM) characterized by a varying degree of muscle weakness and joint contractures and which include Ullrich Congenital Muscular Dystrophy (UCMD) and Bethlem Myopathy (BM). Given that collagen VI is one of the most abundant extracellular matrix proteins in adipose tissue and its emerging role in energy metabolism we hypothesized that collagen VI deficiency might be associated with alterations in adipose tissue distribution and adipokines serum profile. We analyzed body composition by means of dual-energy X-ray absorptiometry in 30 pediatric and adult COL6-RM myopathy patients repres...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
Collagen VI is an extracellular matrix protein expressed in several tissues including skeletal muscl...
International audienceBackground: Dominant and recessive autosomal pathogenic variants in the three ...
Mutations in human collagen VI genes cause a spectrum of musculoskeletal conditions in children and ...
\ua9 2017 Rodr\uedguez, Del Rio Barquero, Ortez, Jou, Vigo, Medina, Febrer, Ramon-Krauel, Diaz-Maner...
Collagen VI mutations lead to disabling myopathies like Bethlem myopathy (BM) and Ullrich congenital...
Mutations in the collagen VI genes cause the Ullrich congenital muscular dystrophy (UCMD), with seve...
Ullrich congenital muscular dystrophy (UCMD) is a genetically and clinically heterogeneous muscle di...
Mutations in the collagen VI genes cause the Ullrich congenital muscular dystrophy (UCMD), with seve...
Collagen VI is an extracellular matrix protein expressed in several tissues including skeletal muscl...
Congenital muscular dystrophies with collagen VI deficiency are inherited muscle disorders with a br...
This study identifies metabolic and protein phenotypic alterations in gastrocnemius, tibialis anteri...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
This study identifies metabolic and protein phenotypic alterations in gastrocnemius, tibialis anteri...
This study identifies metabolic and protein phenotypic alterations in gastrocnemius, tibialis anteri...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
Collagen VI is an extracellular matrix protein expressed in several tissues including skeletal muscl...
International audienceBackground: Dominant and recessive autosomal pathogenic variants in the three ...
Mutations in human collagen VI genes cause a spectrum of musculoskeletal conditions in children and ...
\ua9 2017 Rodr\uedguez, Del Rio Barquero, Ortez, Jou, Vigo, Medina, Febrer, Ramon-Krauel, Diaz-Maner...
Collagen VI mutations lead to disabling myopathies like Bethlem myopathy (BM) and Ullrich congenital...
Mutations in the collagen VI genes cause the Ullrich congenital muscular dystrophy (UCMD), with seve...
Ullrich congenital muscular dystrophy (UCMD) is a genetically and clinically heterogeneous muscle di...
Mutations in the collagen VI genes cause the Ullrich congenital muscular dystrophy (UCMD), with seve...
Collagen VI is an extracellular matrix protein expressed in several tissues including skeletal muscl...
Congenital muscular dystrophies with collagen VI deficiency are inherited muscle disorders with a br...
This study identifies metabolic and protein phenotypic alterations in gastrocnemius, tibialis anteri...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
This study identifies metabolic and protein phenotypic alterations in gastrocnemius, tibialis anteri...
This study identifies metabolic and protein phenotypic alterations in gastrocnemius, tibialis anteri...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
Collagen VI is an extracellular matrix protein expressed in several tissues including skeletal muscl...
International audienceBackground: Dominant and recessive autosomal pathogenic variants in the three ...