Case Reports
doi: 10.1002/mds.26216.
Epub 2015 Jul 21.
De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay
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- PMID: 26195193
- DOI: 10.1002/mds.26216
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Case Reports
De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay
Mov Disord.
2015 Aug.
No abstract available
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