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Comorbidity with autism spectrum disorder (ASD) and other neurodevelopmental conditions has been observed. The genetic etiology is highly heterogeneous. Here, we present three unrelated individuals with CAS and concomitant fine and gross motor involvement but different genetic variants of interest. The DNA of the cases and their parents underwent exome sequencing and variant filtering. Using publicly available data, the genes of interest derived from the variants were investigated for expression rates in the early developing brain. Known and putative protein\u2013protein interactions among the genes of highest confidence were identified. Of 28 variants in 28 different genes, variants with highest confidence were situated in\n                    <jats:italic>FOXN4<\/jats:italic>\n                    ,\n                    <jats:italic>LAMA5<\/jats:italic>\n                    ,\n                    <jats:italic>LAMB1<\/jats:italic>\n                    ,\n                    <jats:italic>LRRK2<\/jats:italic>\n                    , and\n                    <jats:italic>USP17L2<\/jats:italic>\n                    . High gene expression rates in the developing cerebellum were observed for\n                    <jats:italic>LAMA5<\/jats:italic>\n                    and\n                    <jats:italic>LAMB1<\/jats:italic>\n                    . These genes encode the \u03b15 and \u03b21 subunits, respectively, of the heterotrimeric extracellular laminin\u2010511 complex, a major component of the basal membrane in many tissues. Network analysis of the five high\u2010confidence genes required expansion with only one additional gene,\n                    <jats:italic>CDK6<\/jats:italic>\n                    , to arrive at a fully connected network. The addition of four genes and inclusion of transcriptional regulation as an additional edge type allowed connecting all 28 genes of interest to arrive at a dense connectome with 32 nodes and 73 edges, representing a network enrichment with\n                    <jats:italic>p<\/jats:italic>\n                    value of &lt; 0.001, suggesting that our network has significantly more interactions than expected under random conditions. We conclude that high levels of genetic heterogeneity converge on a functional gene network governed by stimulation of cells through laminin\u2010511 with shared direct or regulatory expression in the developing cerebellum and phenotypic overlaps of CAS, ASD, and other neurodevelopmental disorders.\n                  <\/jats:p>","DOI":"10.1155\/crig\/9927839","type":"journal-article","created":{"date-parts":[[2026,2,14]],"date-time":"2026-02-14T06:45:25Z","timestamp":1771051525000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Three Unrelated Children With Childhood Apraxia of Speech: Exome Sequencing and Functional Gene Analysis Imply a Role of Laminin\u2010511 in Early 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