Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference10 articles.
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2. Autosomal dominant acute necrotizing encephalopathy;Neilson;Neurology,2003
3. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2;Neilson;Am J Hum Genet,2009
4. Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy;Loh;Eur J Pediatr,2010
5. Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed family;Gika;Dev Med Child Neurol,2010
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