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has major subject area list
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Developmental Disabilities; Monocarboxylic Acid Transporters; Mutation, Missense; Myopathies, Structural, Congenital
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information resource reference
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A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay. Pediatrics. 2008 Jan; 121(1):e199-202.
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label
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A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay.
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