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X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype.
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X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype.
X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7.
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PubMed
subject areas
Adult
Child, Preschool
Developmental Disabilities
Female
Genetic Diseases, X-Linked
Humans
Intellectual Disability
Male
Monocarboxylic Acid Transporters
Muscle Hypotonia
Muscle Spasticity
Pedigree
Phenotype
Symporters
authors with profiles
Kenton R. Holden