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Secondary biogenic amine deficiencies: genetic etiology,therapeutic interventions,and clinical effects |
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| Authors: | van Karnebeek Clara D. Blydt-Hansen Ingrid Matthews Allison M. Avramovic Vladimir Price Magda Drogemoller Britt Shyr Casper Lee Jessica Mwenifumbo Jill Ghani Aisha Stockler Sylvia Friedman Jan M. Lehman Anna Ross Colin J. Wasserman Wyeth W. Tarailo-Graovac Maja Horvath Gabriella A. |
| Affiliation: | 1.BC Children’s Hospital Research Institute, Vancouver, BC, Canada ;2.Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, Canada ;3.Department of Pediatrics, Amsterdam University Medical Centre, Amsterdam, the Netherlands ;4.Department of Pediatrics, Radboud University Medical Center, Nijmegen, the Netherlands ;5.United for Metabolic Diseases’, Amsterdam, the Netherlands ;6.Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada ;7.Department of Biochemistry, Molecular Biology, and Medical Genetics, Cumming School of Medicine, Alberta Children’s Hospital Research Institute, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, AB, T2N 4N1, Canada ;8.Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada ;9.Adult Metabolic Diseases Clinic, Vancouver General Hospital, Vancouver, Canada ;10.Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada ;11.Biochemical Genetics, BC Children’s Hospital, 4480 Oak Street, Vancouver, BC, V6H 3V4, Canada ; |
| Abstract: | neurogenetics - Monoamine neurotransmitter disorders present predominantly with neurologic features, including dystonic or dyskinetic cerebral palsy and movement disorders. Genetic conditions that... |
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