Associated Papers
Analyses of Human Genetic Data to Identify Clinically Relevant Domains of Neuroligins.
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Genes, 2024
A single-nucleotide substitution mutator phenotype revealed by exome sequencing of human colon adenomas.
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Supplement: 00085472can123869-sup-stab_3_xls_457k_rev.xls › Suppl_Table_S3.csv
Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism.
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Implications of Cell Adhesion Molecules in Autism Spectrum Disorder Pathogenesis.
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