EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome

Affiliations

¹ I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
² Neurological Function Test EMG/EEG Robert Debré Hospital, Paris, France.
³ Molecular Genetics and Biochemistry Unit, HUPC Cochin Hospital, Paris, France.
⁴ Sorbonne University, UPMC Paris 06, INSERM UMRS974, CNRS FRE3617, Center for Research in Myology, 75013, Paris, France.
⁵ National Center of Genotyping, Institute of Genomics, CEA, Evry, France.
⁶ Bioinformatic Platform, Imagine Institute, Sorbonne University, Paris-Descartes, Paris, France.
⁷ I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France. t.gidaro@institut-myologie.org.

Case Reports

Elena Gargaun et al. J Neurol. 2016 Jul.

. 2016 Jul;263(7):1456-8.

doi: 10.1007/s00415-016-8153-9. Epub 2016 May 9.

¹ I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
² Neurological Function Test EMG/EEG Robert Debré Hospital, Paris, France.
³ Molecular Genetics and Biochemistry Unit, HUPC Cochin Hospital, Paris, France.
⁴ Sorbonne University, UPMC Paris 06, INSERM UMRS974, CNRS FRE3617, Center for Research in Myology, 75013, Paris, France.
⁵ National Center of Genotyping, Institute of Genomics, CEA, Evry, France.
⁶ Bioinformatic Platform, Imagine Institute, Sorbonne University, Paris-Descartes, Paris, France.
⁷ I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France. t.gidaro@institut-myologie.org.

No abstract available

References