Distinct neurological disorders with ATP1A3 mutations

Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gene encoding the α3 subunit of Na(+)/K(+)-ATPase, cause both rapid-onset dystonia parkinsonism and alternating hemiplegia of childhood. These discoveries link two clinically distinct neurological diseas...

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Detalhes bibliográficos
Publicado no:Lancet Neurol
Main Authors: Heinzen, Erin L., Arzimanoglou, Alexis, Brashear, Allison, Clapcote, Steven J., Gurrieri, Fiorella, Goldstein, David B., Jóhannesson, Sigurður H., Mikati, Mohamad A., Neville, Brian, Nicole, Sophie, Ozelius, Laurie J., Poulsen, Hanne, Schyns, Tsveta, Sweadner, Kathleen J., van den Maagdenberg, Arn, Vilsen, Bente
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4238309/
https://ncbi.nlm.nih.gov/pubmed/24739246
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1474-4422(14)70011-0
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