(Q46827392)
Statements
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A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay (English)
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Anastasios Papadimitriou
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Alexandra Mihaela Dumitrescu
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Antigone Papavasiliou
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Andreas Fretzayas
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Polyxeni Nicolaidou
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Samuel Refetoff
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1 January 2008
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121
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1
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e199-202
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Identifiers
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