A Novel SCN2A Mutation in Family with Benign Familial Infantile Seizures
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2006.00392.x/fullpdf
Reference8 articles.
1. Benign infantile familial convulsions
2. Benign familial infantile seizures
3. Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16
4. Partial Cosegregation of Familial Hemiplegic Migraine and a Benign Familial Infantile Epileptic Syndrome
5. Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q
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