Associated Papers
Analyses of Human Genetic Data to Identify Clinically Relevant Domains of Neuroligins.
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Genes, 2024
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.
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De novo mutations in moderate or severe intellectual disability.
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25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 266.133
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