Polymicrogyria and Intractable Epilepsy in Siblings With Knobloch Syndrome and Homozygous Mutation of COL18A1 - 07/11/17
Doi : 10.1016/j.pediatrneurol.2017.08.003
Brittany A. Charsar a, * 
, Ethan M. Goldberg, MD, PhD b, c, d
, Ethan M. Goldberg, MD, PhD b, c, d a Department of Neuroscience and Vickie and Jack Farber Institute for Neuroscience, Sidney Kimmel Medical College, and Jefferson College of Biomedical Sciences, Thomas Jefferson University, Philadelphia, Pennsylvania 19107
b Department of Pediatrics, Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
c Department of Neurology, The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania
d Department of Neuroscience, The Perelman School of Medicine at The University of Pennsylvania, Pennsylvania
*Communications should be addressed to:Department of Neuroscience and Vickie and Jack Farber Institute for Neuroscience, Sidney Kimmel Medical College, Thomas Jefferson University, 233 S 10th Street, BLSB Rm 245, Philadelphia, PA 19107.Department of Neuroscience and Vickie and Jack Farber Institute for NeuroscienceSidney Kimmel Medical CollegeThomas Jefferson University233 S 10th Street, BLSB Rm 245PhiladelphiaPA19107
Plan
| Conflicts of interest: None. |
© 2017
Elsevier Inc. Tous droits réservés.
Vol 76
P. 91-92 - novembre 2017 Retour au numéro
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