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Red Blood Cells from Individuals with Lesch-Nyhan Syndrome: Multi-Omics Insights into a Novel S162N Mutation Causing Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency.
Reisz, Julie A; Dzieciatkowska, Monika; Stephenson, Daniel; Gamboni, Fabia; Morton, D Holmes; D'Alessandro, Angelo.
Affiliation
  • Reisz JA; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Dzieciatkowska M; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Stephenson D; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Gamboni F; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Morton DH; Central Pennsylvania Clinic, A Medical Home for Special Children and Adults, Belleville, PA 17004, USA.
  • D'Alessandro A; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Antioxidants (Basel) ; 12(9)2023 Aug 31.
Article in En | MEDLINE | ID: mdl-37760001
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Antioxidants (Basel) Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Antioxidants (Basel) Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza