A novel 5 bp homozygous deletion mutation in ASPH gene associates with Traboulsi syndrome
- 4 March 2019
- journal article
- letter
- Published by Taylor & Francis Ltd in Ophthalmic Genetics
- Vol. 40 (2), 185-187
- https://doi.org/10.1080/13816810.2019.1605390
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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