Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea Syndrome.
Saved in:
| Title: | Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea Syndrome. |
|---|---|
| Authors: | Sklar BA; Department of Ophthalmology, Wills Eye Hospital, Philadelphia PA., Pisuchpen P; Department of Ophthalmology, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand., Bareket M; Department of Ophthalmology, Kaplan Medical Center, Rehovot, Israel., Milman T; Eye Pathology Department, Wills Eye Hospital, Philadelphia PA., Eagle RC Jr; Eye Pathology Department, Wills Eye Hospital, Philadelphia PA., Minor J; Pediatric and Adult Strabismus Service, Wills Eye Hospital, Philadelphia PA., Procopio R; Ocular Genetics, Wills Eye Hospital, Philadelphia PA., Capasso J; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, Clinical Genetics, Golisano Children's Hospital, University of Rochester, Rochester, NY; and., Levin AV; Pediatric Ophthalmology and Ocular Genetics, Flaum Eye Institute, Clinical Genetics, Golisano Children's Hospital, University of Rochester, Rochester, NY; and., Hammersmith K; Cornea Service, Wills Eye Hospital, Philadelphia PA. |
| Source: | Cornea [Cornea] 2023 Dec 01; Vol. 42 (12), pp. 1572-1577. Date of Electronic Publication: 2023 Sep 15. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8216186 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1536-4798 (Electronic) Linking ISSN: 02773740 NLM ISO Abbreviation: Cornea Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
