[HTML] nature.com

[HTML][HTML] Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast… - Cell Death & …, 2021 - nature.com
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …
被引用次数：50 相关文章

Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast… - Cell Death & …, 2020 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> SEPN1-related myopathy (SEPN1-RM) is a
muscle disorder due to mutations of the< jats: italic> SEPN1</jats: italic> gene, which is …

Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast… - CELL DEATH AND …, 2021 - ora.uniurb.it
: SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the SEPN1
gene, which is characterized by muscle weakness and fatigue leading to scoliosis and life …

Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy… - Cell death and …, 2021 - pubmed.ncbi.nlm.nih.gov
SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the SEPN1
gene, which is characterized by muscle weakness and fatigue leading to scoliosis and life …

Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy… - Cell Death and …, 2021 - utsouthwestern.elsevierpure.com
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …

Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast… - CELL DEATH AND …, 2021 - sfera.unife.it
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …
[PDF] academia.edu

[PDF][PDF] Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast, E Varone… - 2020 - academia.edu
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …
[PDF] unife.it

[PDF][PDF] Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast, E Varone… - 2020 - sm.unife.it
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …
[PDF] myoparis.fr

[PDF][PDF] Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy

A Filipe, A Chernorudskiy, S Arbogast… - Cell Death & …, 2021 - myoparis.fr
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …

Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy.

A Filipe, A Chernorudskiy, S Arbogast… - Cell Death and …, 2020 - europepmc.org
Abstract SEPN1-related myopathy (SEPN1-RM) is a muscle disorder due to mutations of the
SEPN1 gene, which is characterized by muscle weakness and fatigue leading to scoliosis …