Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 Mutation
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Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference30 articles.
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2. Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene;CE Schwartz;Am J Hum Genet,2005
3. X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene;K Brockmann;J Neurol,2005
4. X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype;KR Holden;J Child Neurol,2005
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