dc.contributor
Institut Català de la Salut
dc.contributor
[Oghabian Ali] Folkhälsan Research Center, Helsinki, Finland. Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland. [Jonson PH, Gayathri SN] Folkhälsan Research Center, Helsinki, Finland. Department of Medical Genetics, University of Helsinki, Helsinki, Finland. [Johari M] Folkhälsan Research Center, Helsinki, Finland. Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia. [Nippala E] Folkhälsan Research Center, Helsinki, Finland. [Gomez Andres D, Munell F] Unitat de Malalties Neuromusculars, Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Neurologia Pediàtrica, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Camacho Soriano J] Servei d’Anatomia Patològica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Sanchez Duran MA] Unitat de Diagnòstic Prenatal, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Sinisalo J] Universitat Autònoma de Barcelona, Bellaterra, Spain. Servei d’Obstetrícia, Unitat de Medicina Fetal, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.contributor
Vall d'Hebron Barcelona Hospital Campus
dc.contributor.author
Oghabian, Ali
dc.contributor.author
Jonson, Per Harald
dc.contributor.author
Gayathri, Swethaa Natraj
dc.contributor.author
Johari, Mridul
dc.contributor.author
Nippala, Ella
dc.contributor.author
Gómez-Andrés, David
dc.contributor.author
Munell Casadesus, Francina
dc.contributor.author
Camacho, Jessica
dc.contributor.author
Sanchez-Duran, M Angeles
dc.contributor.author
Sinisalo, Juha
dc.date.accessioned
2025-05-16T13:54:27Z
dc.date.available
2025-05-16T13:54:27Z
dc.date.issued
2025-05-15T08:04:03Z
dc.date.issued
2025-05-15T08:04:03Z
dc.date.issued
2025-04-07
dc.identifier
Oghabian A, Jonson PH, Gayathri SN, Johari M, Nippala E, Andres DG, et al. Correction: OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development. Skelet Muscle. 2025 Apr 7;15:10.
dc.identifier
http://hdl.handle.net/11351/13091
dc.identifier
10.1186/s13395-025-00380-8
dc.identifier
001465161100001
dc.identifier.uri
http://hdl.handle.net/11351/13091
dc.description.abstract
Inclusión de exones; Desarrollo muscular; Enfermedades neuromusculares
dc.description.abstract
Inclusió d'exons; Desenvolupament muscular; Malalties neuromusculars
dc.description.abstract
Exon inclusion; Muscle development; Neuromuscular diseases
dc.format
application/pdf
dc.relation
Skeletal Muscle;15
dc.relation
https://doi.org/10.1186/s13395-025-00380-8
dc.rights
Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Malalties neuromusculars - Aspectes genètics
dc.subject
Empalmament (Genètica)
dc.subject
Regulació genètica
dc.subject
Infants nadons
dc.subject
PHENOMENA AND PROCESSES::Physiological Phenomena::Growth and Development::Morphogenesis::Embryonic and Fetal Development::Organogenesis::Musculoskeletal Development::Muscle Development
dc.subject
PHENOMENA AND PROCESSES::Genetic Phenomena::Gene Expression Regulation::RNA Processing, Post-Transcriptional::RNA Splicing::Alternative Splicing
dc.subject
DISEASES::Nervous System Diseases::Neuromuscular Diseases
dc.subject
Other subheadings::Other subheadings::Other subheadings::/genetics
dc.subject
PHENOMENA AND PROCESSES::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Gene Components::Exons
dc.subject
ANATOMY::Musculoskeletal System::Muscles::Myocardium
dc.subject
PHENOMENA AND PROCESSES::Genetic Phenomena::Gene Expression Regulation::Gene Expression Regulation, Developmental
dc.subject
NAMED GROUPS::Persons::Age Groups::Infant::Infant, Newborn
dc.subject
FENÓMENOS Y PROCESOS::fenómenos fisiológicos::crecimiento y desarrollo::morfogénesis::desarrollo embrionario y fetal::organogénesis::desarrollo musculoesquelético::desarrollo muscular
dc.subject
FENÓMENOS Y PROCESOS::fenómenos genéticos::regulación de la expresión génica::procesamiento postranscripcional del ARN::empalme de ARN::empalme alternativo
dc.subject
ENFERMEDADES::enfermedades del sistema nervioso::enfermedades neuromusculares
dc.subject
Otros calificadores::Otros calificadores::Otros calificadores::/genética
dc.subject
FENÓMENOS Y PROCESOS::fenómenos genéticos::estructuras genéticas::genoma::componentes genómicos::genes::componentes génicos::exones
dc.subject
ANATOMÍA::sistema musculoesquelético::músculos::miocardio
dc.subject
FENÓMENOS Y PROCESOS::fenómenos genéticos::regulación de la expresión génica::regulación de la expresión génica en el desarrollo
dc.subject
DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::lactante::recién nacido
dc.title
Correction: OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion
