Spauschus, A and Eunson, L and Hanna, MG and Kullmann, DM (1999) Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy. MOLECULAR AND FUNCTIONAL DIVERSITY OF ION CHANNELS AND RECEPTORS , 868 442 - 446.
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| Type: | Article |
|---|---|
| Title: | Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy |
| Location: | NEW YORK, NY |
| Keywords: | POTASSIUM CHANNEL GENE, MYOKYMIA SYNDROME, FAMILIES, KV1.1, ALTER |
| UCL classification: | UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology > Clinical and Experimental Epilepsy UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology > Molecular Neuroscience |
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