Jasmine Lin
3PUBLICATIONS
8CO-AUTHORS
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Publications (3)
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|Jul 05, 2024
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells.Shiyu Luo, Bilal Alwattar, Qifei Li
|Jun 29, 2022
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene.Boxun Zhao, Jill A Madden, Jasmine Lin
|Dec 24, 2021
Reanalysis of Exome Data Identifies Novel SLC25A46 Variants Associated with Leigh Syndrome.Qifei Li, Jill A Madden, Jasmine Lin
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