System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution ; volume:14 ; number:1 ; day:16 ; month:5 ; year:2024 ; pages:1-10 ; date:12.2024
Scientific reports ; 14, Heft 1 (16.5.2024), 1-10, 12.2024
- Creator
-
Ozisik, Ozan
Gorokhova, Svetlana
Cerino, Mathieu
Bartoli, Marc
Baudot, Anaïs
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-024-60761-9
- URN
-
urn:nbn:de:101:1-2407252117145.142002473260
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:54 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ozisik, Ozan
- Gorokhova, Svetlana
- Cerino, Mathieu
- Bartoli, Marc
- Baudot, Anaïs
- SpringerLink (Online service)
Other Objects (12)
Acute muscular weakness in children
Metabolome and Proteome Based Analysis of Muscular Dystrophies
Timed immersion expiration measures in patients with muscular dystrophies
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders
Respiratory muscle weakness in facioscapulohumeral muscular dystrophy
Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies
Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies
Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis
Comparison of splicing and nuclear envelope alterations in three muscular dystrophies
Advanced gene-targeting therapies for motor neuron diseases and muscular dystrophies
Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies
Acute muscular weakness in children
Metabolome and Proteome Based Analysis of Muscular Dystrophies
Timed immersion expiration measures in patients with muscular dystrophies
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders
Respiratory muscle weakness in facioscapulohumeral muscular dystrophy
Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies
Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies
Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis
Comparison of splicing and nuclear envelope alterations in three muscular dystrophies
Advanced gene-targeting therapies for motor neuron diseases and muscular dystrophies
Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies
Acute muscular weakness in children
Metabolome and Proteome Based Analysis of Muscular Dystrophies
Timed immersion expiration measures in patients with muscular dystrophies
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders
Respiratory muscle weakness in facioscapulohumeral muscular dystrophy
Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies
Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies
Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis
Comparison of splicing and nuclear envelope alterations in three muscular dystrophies
Advanced gene-targeting therapies for motor neuron diseases and muscular dystrophies