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Association of EFEMP1 with juvenile-onset open angle glaucoma in a patient with concomitant COL11A1 -related Stickler syndrome.

Viney GuptaBindu I SomarajanShikha GuptaKarthikeyan MahalingamManoj KumarAbhishek Singh
Published in: Ophthalmic genetics (2022)
This is a rare association of EFEMP1 and COL11A1 sequence variants in a JOAG patient with STL. The study also reiterates the association of JOAG with EFEMP1, which should be looked for, especially in families with autosomal dominant JOAG.
Keyphrases
  • case report
  • gene expression
  • copy number
  • genome wide