The functional enrichment of whole exome sequencing (WES) data suggests that the canonical Wnt pathway plays a role in Chiari malformation type I with possible oligogenic mechanisms

Maria Cerminara, Patrizia De Marco, Michele Iacomino,Diego Vozzi, Valeria Capra,Marco Fontana, Marco Pavanello, Gianluca Piatelli,Federico Zara,Aldamaria Puliti

EUROPEAN JOURNAL OF HUMAN GENETICS(2024)

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