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Intellectual Disability and Brain Creatine Deficit: Phenotyping of the Genetic Mouse Model for GAMT Deficiency.
Rossi, Luigia; Nardecchia, Francesca; Pierigè, Francesca; Ventura, Rossella; Carducci, Claudia; Leuzzi, Vincenzo; Magnani, Mauro; Cabib, Simona; Pascucci, Tiziana.
Affiliation
  • Rossi L; Department of Biomolecular Sciences, University of Urbino "Carlo Bo", 61029 Urbino, Italy.
  • Nardecchia F; EryDel SpA, Via Sasso 36, 61029 Urbino, Italy.
  • Pierigè F; Division of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University, 00185 Rome, Italy.
  • Ventura R; Department of Biomolecular Sciences, University of Urbino "Carlo Bo", 61029 Urbino, Italy.
  • Carducci C; Department of Psychology and "Daniel Bovet" Center, Sapienza University, 00184 Rome, Italy.
  • Leuzzi V; IRCCS Fondazione Santa Lucia, 00142 Rome, Italy.
  • Magnani M; Department of Experimental Medicine, Sapienza University, 00161 Rome, Italy.
  • Cabib S; Division of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University, 00185 Rome, Italy.
  • Pascucci T; Department of Biomolecular Sciences, University of Urbino "Carlo Bo", 61029 Urbino, Italy.
Genes (Basel) ; 12(8)2021 08 02.
Article in En | MEDLINE | ID: mdl-34440375
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Brain / Creatine / Guanidinoacetate N-Methyltransferase / Language Development Disorders / Intellectual Disability / Movement Disorders Limits: Animals Language: En Journal: Genes (Basel) Year: 2021 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Brain / Creatine / Guanidinoacetate N-Methyltransferase / Language Development Disorders / Intellectual Disability / Movement Disorders Limits: Animals Language: En Journal: Genes (Basel) Year: 2021 Document type: Article Affiliation country: Country of publication: