Last Updated: 09/26/2026
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Found 3 publications
Abnormal Meibum Is Associated With SREBF1 Mutation And IFAP Syndrome-2.
Journal: medRxiv : the preprint server for health sciences
Published: August 08, 2025
Abnormal meibum is associated with SREBF1 mutation and IFAP Syndrome-2.
Journal: Experimental eye research
Published: July 17, 2025
Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects.
Journal: Human genetics
Published: February 17, 2021
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Last Updated: 09/26/2026