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Splicing in two skeletal muscle transcripts correlates with clinical phenotype in myotonic dystrophy type 1 patients.
Sedehizadeh, Saam; Wojciechowska, Marzena; Ketley, Ami; Brook, J David; Maddison, Paul.
Affiliation
  • Sedehizadeh S; Department of Neurology, Queen's Medical Centre, Nottingham University Hospitals NHS Trust, Nottingham, UK. saam.sedehizadeh@nhs.net.
  • Wojciechowska M; Department of Molecular Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704, Poznan, Poland.
  • Ketley A; School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, UK.
  • Brook JD; School of Life Sciences, Queen's Medical Centre, University of Nottingham, Nottingham, UK.
  • Maddison P; Department of Neurology, Queen's Medical Centre, Nottingham University Hospitals NHS Trust, Nottingham, UK.
J Neurol ; 269(5): 2784-2787, 2022 05.
Article in En | MEDLINE | ID: mdl-34981221
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myotonic Dystrophy Limits: Humans Language: En Journal: J Neurol Year: 2022 Document type: Article Affiliation country: Reino Unido
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myotonic Dystrophy Limits: Humans Language: En Journal: J Neurol Year: 2022 Document type: Article Affiliation country: Reino Unido