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Amedeo Smart

Independent Medical Education


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Su J, Tao Y, Zhang L, Luo J, et al. Identification of a new frameshift homozygous variant of PEX3 gene in a preterm infant with profound global developmental delay and bilateral ptosis: a case report and updated literature review. BMC Pediatr 2026 Jan 6. doi: 10.1186/s12887-025-06472.
PMID: 41495707


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