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Supplementary Material for: THUMPD1-Related Neurodevelopmental Disorder: A Novel Homozygous Loss-of-Function Variant with an Unusual Skeletal Phenotype: A Case Report

Name: Supplementary Material for: THUMPD1-Related Neurodevelopmental Disorder: A Novel Homozygous Loss-of-Function Variant with an Unusual Skeletal Phenotype: A Case Report
License: Open Access

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medicine, medicine

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