Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy

Nathalie Doorenweerd*, Ahmed Mahfouz, Maaike van Putten, Rajaram Kaliyaperumal, Peter A. C. t' Hoen, Jos G. M. Hendriksen, Annemieke M. Aartsma-Rus, Jan J. G. M. Verschuuren, Erik H. Niks, Marcel J. T. Reinders, Hermien E. Kan, Boudewijn P. F. Lelieveldt

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Article number12575
Number of pages12
JournalScientific Reports
Volume7
DOIs
Publication statusPublished - 3 Oct 2017

Keywords

  • DE-NOVO MUTATIONS
  • CENTRAL-NERVOUS-SYSTEM
  • DEFICIENT MDX MICE
  • GLYCOPROTEIN COMPLEX
  • HUMAN BRAIN
  • AUTISM
  • GENE
  • MOUSE
  • DISORDERS
  • PROMOTER

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