Associated Papers
Analysis of candidate variants in a Chinese family with monozygotic twins with keratoconus: a case report.
Song C et al.
Ophthalmic Genetics, 2025
39544142 (PubMed )
Supplement: supplement_1.xlsx › Sheet1
Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82.
Erjavec SO et al.
Nature Communications, 2022
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