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C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases.
Shinbashi, Meagan; Jewell, Ann; Randolph, Jessica; Couser, Natario.
Affiliation
  • Shinbashi M; Virginia Commonwealth University School of Medicine Virginia Richmond USA.
  • Jewell A; Department of Human and Molecular Genetics Virginia Commonwealth University School of Medicine Virginia Richmond USA.
  • Randolph J; Department of Human and Molecular Genetics Virginia Commonwealth University School of Medicine Virginia Richmond USA.
  • Couser N; Department of Ophthalmology Virginia Commonwealth University School of Medicine Virginia Richmond USA.
Clin Case Rep ; 11(3): e7110, 2023 Mar.
Article in En | MEDLINE | ID: mdl-36950666
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Case Rep Year: 2023 Document type: Article Country of publication: Reino Unido
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Case Rep Year: 2023 Document type: Article Country of publication: Reino Unido