Lv52
1050 积分 2024-01-28 加入
MBD5 and MBD6 interact with the human PR‐DUB complex through their methyl‐CpG‐binding domain
8小时前
待确认
Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies
10小时前
待确认
A Unique Case of MBD5 and CCM2 Deletions Leading to a Severe Neurological Phenotype With Prolonged Status Epilepticus
21小时前
已完结
MBD5‐related intellectual disability in a Vietnamese child
11天前
已完结
[Clinical phenotypes and genetic features of epilepsy children with MBD5 gene variants]
14天前
已完结
Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?
14天前
已完结
Unraveling the genetic basis of epilepsy: Recent advances and implications for diagnosis and treatment
15天前
已完结
Novel homozygous AP3B2 mutations in four individuals with developmental and epileptic encephalopathy: A rare clinical entity
22天前
已完结
The expanding spectrum of antibody-associated cerebellar ataxia: report of two new cases of anti-AP3B2 ataxia
22天前
已完结
Obsessive–compulsive symptoms and 15q11.2q13.1 duplication syndrome
22天前
已完结
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