QuickView for tbc1d24 protein human

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1. Myoclonic Status Epilepticus in TBC1D24-Related Developmental/Epileptic Encephalopathy (DEE).
2. A personal life experience as a parent of children with TBC1D24-related developmental and epileptic …
3. Investigation of a novel TBC1D24 variation causing autosomal dominant non-syndromic hearing loss.
4. Case report of a novel mutation in the TNC gene in Chinese patients with nonsyndromic hearing loss.
5. Alternating Hemiplegia of Childhood in a Child Harboring a Novel TBC1D24 Mutation: Case Report and L…

There were no clinical trials for tbc1d24 protein human