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NMNAT1-ASSOCIATED CONE-ROD DYSTROPHY: EVIDENCE FOR A SPECTRUM OF FOVEAL MALDEVELOPMENT.
Bedoukian, Emma C; Zhu, Xiaosong; Serrano, Leona W; Scoles, Drew; Aleman, Tomas S.
Affiliation
  • Bedoukian EC; Divisions of Human Genetics and.
  • Zhu X; Ophthalmology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; the.
  • Serrano LW; Scheie Eye Institute at the Perelman Center for Advanced Medicine and the.
  • Scoles D; Ophthalmology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA; the.
  • Aleman TS; Divisions of Human Genetics and.
Retin Cases Brief Rep ; 16(3): 385-392, 2022 May 01.
Article in En | MEDLINE | ID: mdl-32150116
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cone-Rod Dystrophies / Nicotinamide-Nucleotide Adenylyltransferase Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Retin Cases Brief Rep Year: 2022 Document type: Article Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cone-Rod Dystrophies / Nicotinamide-Nucleotide Adenylyltransferase Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Retin Cases Brief Rep Year: 2022 Document type: Article Country of publication: United States