Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations.
Identifieur interne : 000E92 ( Main/Exploration ); précédent : 000E91; suivant : 000E93Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations.
Auteurs : Athanasia Alexoudi [Allemagne] ; Susanne A. SchneiderSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.
PubMed: 23460948
Affiliations:
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Le document en format XML
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