(Q51862552)
Statements
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Novel CLN8 mutations confirm the clinical and ethnic diversity of late infantile neuronal ceroid lipofuscinosis. (English)
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K Reinhardt
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M Grapp
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K Schlachter
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W Brück
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J Gärtner
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R Steinfeld
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5 October 2009
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77
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1
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79-85
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Identifiers
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