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UnknownFirst Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations.
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S-EPMC10090972 | biostudies-literature
UnknownExpanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
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S-EPMC11739428 | biostudies-literature
UnknownGenetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
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S-EPMC6685441 | biostudies-literature
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