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ALDH1A2-related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway.
Leon, Eyby; Nde, Claris; Ray, Randall S; Preciado, Diego; Zohn, Irene E.
Affiliation
  • Leon E; Rare Disease Institute, Children's National Hospital, Washington, DC, USA.
  • Nde C; Center for Genetic Medicine, Children's National Hospital, Washington, DC, USA.
  • Ray RS; Rare Disease Institute, Children's National Hospital, Washington, DC, USA.
  • Preciado D; Division of Pediatric Otolaryngology, Children's National Hospital, Washington, DC, USA.
  • Zohn IE; Center for Genetic Medicine, Children's National Hospital, Washington, DC, USA.
Am J Med Genet A ; 191(1): 90-99, 2023 Jan.
Article in En | MEDLINE | ID: mdl-36263470
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tretinoin Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2023 Type: Article Affiliation country: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tretinoin Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2023 Type: Article Affiliation country: United States