Atypical Rett Syndrome and Intractable Epilepsy With Novel
GRIN2B
Mutation
Child Neurol Open
.
2018 Aug 23:5:2329048X18787946.
doi: 10.1177/2329048X18787946.
eCollection 2018.
Authors
Paulina Kyriakopoulos
1
2
,
Vanda McNiven
3
2
,
Melissa T Carter
4
,
Peter Humphreys
5
,
David Dyment
4
,
Tadeu A Fantaneanu
1
Affiliations
1
Division of Neurology, The Ottawa Hospital Civic Campus, Ottawa, Ontario, Canada.
2
co-authors who contributed equally.
3
Division of Clinical Genetics and Metabolics, SickKids, Toronto, Ontario, Canada.
4
Department of Genetics, The Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
5
Division of Neurology, Department of Pediatrics, The Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
PMID:
30151416
PMCID:
PMC6108011
DOI:
10.1177/2329048X18787946
No abstract available
Keywords:
GRIN2B; atypical Rett syndrome; epilepsy; memantine.