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Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in ASPH.
Ophthalmic Genet. 2021 Aug;42(4):493-499. doi: 10.1080/13816810.2021.1923039. Epub 2021 May 21.
Ophthalmic Genet. 2021.
PMID: 34018898
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