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Biochemical features of primary cells from a pediatric patient with a gain-of-function ODC1 genetic mutation.
Schultz, Chad R; Bupp, Caleb P; Rajasekaran, Surender; Bachmann, André S.
Affiliation
  • Schultz CR; Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, MI, U.S.A.
  • Bupp CP; Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, MI, U.S.A.
  • Rajasekaran S; Medical Genetics, Spectrum Health and Helen DeVos Children's Hospital, Grand Rapids, MI, U.S.A.
  • Bachmann AS; Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, MI, U.S.A.
Biochem J ; 476(14): 2047-2057, 2019 07 24.
Article in En | MEDLINE | ID: mdl-31249027
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / Dermis / Dicarboxylic Acid Transporters / Mitochondrial Membrane Transport Proteins / Alopecia / Fibroblasts / Gain of Function Mutation Limits: Child, preschool / Female / Humans Language: En Journal: Biochem J Year: 2019 Document type: Article Affiliation country: United States Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / Dermis / Dicarboxylic Acid Transporters / Mitochondrial Membrane Transport Proteins / Alopecia / Fibroblasts / Gain of Function Mutation Limits: Child, preschool / Female / Humans Language: En Journal: Biochem J Year: 2019 Document type: Article Affiliation country: United States Country of publication: United kingdom