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Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias
Download from doi.orgBiallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy
UploadP016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report
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