Early-Onset Epileptic Encephalopathies with STXBPl Mutations
Researchers at the Department of Molecular Genetics, University of Antwerp, and other centers in Belgium, The Netherlands, and Melbourne, Australia, analyzed the clinical phenotypes associated with STXBPl mutations in a cohort of 106 patients with unexplained early-onset epileptic encephalopathies.
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Format: | Article |
Language: | English |
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Pediatric Neurology Briefs Publishers
2010-12-01
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Series: | Pediatric Neurology Briefs |
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Online Access: | https://www.pediatricneurologybriefs.com/articles/714 |
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author | J Gordon Millichap |
author_facet | J Gordon Millichap |
author_sort | J Gordon Millichap |
collection | DOAJ |
description | Researchers at the Department of Molecular Genetics, University of Antwerp, and other centers in Belgium, The Netherlands, and Melbourne, Australia, analyzed the clinical phenotypes associated with STXBPl mutations in a cohort of 106 patients with unexplained early-onset epileptic encephalopathies. |
first_indexed | 2024-04-13T03:44:00Z |
format | Article |
id | doaj.art-c68f4b013063401bbbbc2e8e17e13454 |
institution | Directory Open Access Journal |
issn | 1043-3155 2166-6482 |
language | English |
last_indexed | 2024-04-13T03:44:00Z |
publishDate | 2010-12-01 |
publisher | Pediatric Neurology Briefs Publishers |
record_format | Article |
series | Pediatric Neurology Briefs |
spelling | doaj.art-c68f4b013063401bbbbc2e8e17e134542022-12-22T03:04:04ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64822010-12-012412899010.15844/pedneurbriefs-24-12-1700Early-Onset Epileptic Encephalopathies with STXBPl MutationsJ Gordon Millichap0Northwestern University Feinberg School of MedicineResearchers at the Department of Molecular Genetics, University of Antwerp, and other centers in Belgium, The Netherlands, and Melbourne, Australia, analyzed the clinical phenotypes associated with STXBPl mutations in a cohort of 106 patients with unexplained early-onset epileptic encephalopathies.https://www.pediatricneurologybriefs.com/articles/714early myoclonic encephalopathyearly-onset epileptic encephalopathyohtahara syndrome |
spellingShingle | J Gordon Millichap Early-Onset Epileptic Encephalopathies with STXBPl Mutations Pediatric Neurology Briefs early myoclonic encephalopathy early-onset epileptic encephalopathy ohtahara syndrome |
title | Early-Onset Epileptic Encephalopathies with STXBPl Mutations |
title_full | Early-Onset Epileptic Encephalopathies with STXBPl Mutations |
title_fullStr | Early-Onset Epileptic Encephalopathies with STXBPl Mutations |
title_full_unstemmed | Early-Onset Epileptic Encephalopathies with STXBPl Mutations |
title_short | Early-Onset Epileptic Encephalopathies with STXBPl Mutations |
title_sort | early onset epileptic encephalopathies with stxbpl mutations |
topic | early myoclonic encephalopathy early-onset epileptic encephalopathy ohtahara syndrome |
url | https://www.pediatricneurologybriefs.com/articles/714 |
work_keys_str_mv | AT jgordonmillichap earlyonsetepilepticencephalopathieswithstxbplmutations |