Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN in-silico structural analysis.
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Vecchio D, et al. Among authors: nucci cg.
Front Genet. 2024 Dec 11;15:1477940. doi: 10.3389/fgene.2024.1477940. eCollection 2024.
Front Genet. 2024.
PMID: 39722796
Free PMC article.