Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity
NIH| Nervous System Channelopathies: Pathogenesis &Treatment
Authors: Tracey D, Graves; Michael G, Hanna;
pmid: 18446307
Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity
Related Organizations
- University College London United Kingdom
- UCL Queen Square Institute of Neurology United Kingdom
Keywords
Adult, Family Health, Male, Adolescent, DNA Mutational Analysis, Middle Aged, Excitatory Amino Acid Transporter 1, Mutation, Humans, Ataxia, Female, Calcium Channels, Child
Adult, Family Health, Male, Adolescent, DNA Mutational Analysis, Middle Aged, Excitatory Amino Acid Transporter 1, Mutation, Humans, Ataxia, Female, Calcium Channels, Child
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