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Journal Article
Neurology, ISSN 0028-3878, 2010, Volume 75, Issue 1, pp. 64 - 71
Journal Article
Human Brain Mapping, ISSN 1065-9471, 03/2017, Volume 38, Issue 3, pp. 1532 - 1540
Journal Article
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 06/2019, Volume 181, Issue 2, pp. 226 - 229
Aromatic l‐amino acid decarboxylase deficiency (AADCD) is a rare inherited disease prevalent in South East Asia. This disease is due to the founder mutation... 
clinical trial | splicing mutation | adeno‐associated virus | gene therapy | animal model | AADC deficiency | adeno-associated virus | Medicine, Experimental | Medical research | Amino acids | Biological products | Analysis | Phenotypes | Silicone resins | Acids | Medical services | Aromatic-L-amino-acid decarboxylase | Mutation | Gene therapy | Polydimethyl siloxanes | Patients | Hereditary diseases
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2017, Volume 12, Issue 1, p. 12
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Journal Article
Pediatric Neurology, ISSN 0887-8994, 12/2019
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