Your browser doesn't support javascript.
loading
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.
Afiliación
  • 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 en En | MEDLINE | ID: mdl-34981221
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Distrofia Miotónica Límite: Humans Idioma: En Revista: J Neurol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Distrofia Miotónica Límite: Humans Idioma: En Revista: J Neurol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido