The expanding spectrum of ATP1A3 related disease
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Reference14 articles.
1. Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A3;Sabouraud;Eur J Paediatr Neurol,2019
2. Diagnosis and treatment of alternating hemiplegia of childhood;Masoud;Curr Treat Options Neurol,2017
3. Neurological disease mutations of alpha3 Na(+),K(+)-ATPase: structural and functional perspectives and rescue of compromised function;Holm;Biochim Biophys Acta,2016
4. Distinct neurological disorders with ATP1A3 mutations;Heinzen;Lancet Neurol,2014
5. Functional consequences of the CAPOS mutation E818K of Na+,K+-ATPase;Roenn;J Biol Chem,2019
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