Lv1
50 积分 2024-11-17 加入
New Face for Chromatin‐Related Mesenchymal Modulator: n‐CHD9 Localizes to Nucleoli and Interacts With Ribosomal Genes
4天前
已完结
NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation
10天前
已完结
Pediatric Epilepsy Management: Special Considerations
1个月前
已关闭
Childhood epilepsy
1个月前
已关闭
Effect of inbreeding on intellectual disability revisited by trio sequencing
4个月前
已完结
Neuronal connectivity, behavioral, and transcriptional alterations associated with the loss of MARK2
4个月前
已完结
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease
5个月前
已完结
Trinucleotide Repeat Disorders
5个月前
已完结
Protective effect of CACNA1A deficiency in oligogenic refractory epilepsy with CACNA1A‐CELSR2 digenic mutations
6个月前
已完结
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders
6个月前
已完结
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