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2022-11-20 加入
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The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children
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Genetic analysis of developmental and epileptic encephalopathy caused by novel biallelic SZT2 gene mutations in three Chinese Han infants: a case series and literature review
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Giant ankyrin-B suppresses stochastic collateral axon branching through direct interaction with microtubules
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Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations
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