Lv1
20 积分 2022-02-22 加入
Compound heterozygous mutations in the SSPOP gene lead to epilepsy and developmental disorders
4小时前
待确认
Association of increased cortical thickness and cognitive impairment in patients with Kallmann syndrome
5小时前
待确认
Potassium Channelopathies and Precision Medicine Approaches in Epilepsy: A Systematic Review of Personalized Treatment Strategies
1个月前
已完结
Gene therapy with covalently closed-end AAV vector for spinal muscular atrophy
1个月前
已完结
Hypercalcaemia in a Patient with 2p13.2-p16.1 Duplication
10个月前
已完结
A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizures
11个月前
已完结
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