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This page is a summary of: Reanalysis of Whole-Exome Sequencing Data of an Infant with Suspected Diagnosis of Jeune Syndrome Revealed a Likely Pathogenic Variant in <i>GRK2:</i> A Newly Associated Gene for Jeune Syndrome Phenotype, Molecular Syndromology, November 2023, Karger Publishers,
DOI: 10.1159/000534031.
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