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MIM:607631 - EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1; EJA1
Xenbase Genes: clcn2, efhc1
Human Disease Resource: MIM
MONDO:0020772 - epilepsy, juvenile absence, susceptibility to, 1 |
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MONDO:0020772 - epilepsy, juvenile absence, susceptibility to, 1 |