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Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy.
Waldrop, Megan A; Moore, Steven A; Mathews, Katherine D; Darbro, Benjamin W; Medne, Livja; Finkel, Richard; Connolly, Anne M; Crawford, Thomas O; Drachman, Daniel; Wein, Nicolas; Habib, Ali A; Krzesniak-Swinarska, Monika A; Zaidman, Craig M; Collins, James J; Jokela, Manu; Udd, Bjarne; Day, John W; Ortiz-Guerrero, Gloria; Statland, Jeff; Butterfield, Russell J; Dunn, Diane M; Weiss, Robert B; Flanigan, Kevin M.
Affiliation
  • Waldrop MA; The Center for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Moore SA; Department of Neurology, The Ohio State University, Columbus, Ohio, USA.
  • Mathews KD; Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
  • Darbro BW; Department of Pathology, The University of Iowa, Iowa City, Iowa, USA.
  • Medne L; Depatment of Pediatrics, The University of Iowa, Iowa City, Iowa, USA.
  • Finkel R; Depatment of Pediatrics, The University of Iowa, Iowa City, Iowa, USA.
  • Connolly AM; Department of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Crawford TO; Department of Neurology, Nemours Children's Hospital, Orlando, Florida, USA.
  • Drachman D; Department of Neurology, Washington University, Saint Louis, Missouri, USA.
  • Wein N; Department of Neurology, Johns Hopkins University, Baltimore, Maryland, USA.
  • Habib AA; Department of Neurology, Johns Hopkins University, Baltimore, Maryland, USA.
  • Krzesniak-Swinarska MA; The Center for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Zaidman CM; Department of Neurology, Columbia University, New York, New York, USA.
  • Collins JJ; Department of Neurology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
  • Jokela M; Department of Neurology, Washington University, Saint Louis, Missouri, USA.
  • Udd B; Department of Pediatric Neurology, Mercy Hospitals, Springfield, Missouri, USA.
  • Day JW; Neuromuscular Research Center, Tampere University Hospital and University of Tampere, Tampere, Finland.
  • Ortiz-Guerrero G; Division of Clinical Neurosciences, Turku University Hospital and University of Turku, Turku, Finland.
  • Statland J; Neuromuscular Research Center, Tampere University Hospital and University of Tampere, Tampere, Finland.
  • Butterfield RJ; Department of Neurology, University of Minnesota Medical Center, Minneapolis, Minnesota, USA.
  • Dunn DM; Department of Neurology, University of Kansas, Kansas City, Kansas, USA.
  • Weiss RB; Department of Neurology, University of Kansas, Kansas City, Kansas, USA.
  • Flanigan KM; Department of Pediatrics, The University of Utah School of Medicine, Salt Lake City, Utah, USA.
Hum Mutat ; 43(4): 511-528, 2022 04.
Article de En | MEDLINE | ID: mdl-35165973
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Dystrophine / Myopathie de Duchenne Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Hum Mutat Sujet du journal: GENETICA MEDICA Année: 2022 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Dystrophine / Myopathie de Duchenne Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Hum Mutat Sujet du journal: GENETICA MEDICA Année: 2022 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique