Publication | Closed Access
Two Japanese cases of epileptic encephalopathy associated with an FGF12 mutation
19
Citations
7
References
2018
Year
Epileptic EncephalopathyMendelian DisorderNeurological DisorderFgf12 MutationGenetic DisorderPathologyNeurologyNeuroscienceNeuropathologyMedicineJapanese CasesNeurogenetics
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