(Q34372978)
Statements
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Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter (English)
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Thierry Dupré
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Véronique Piller
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Friedrich Piller
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Jean-Jacques Candelier
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Catherine Trichet
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Gil Tchernia
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Rafael Oriol
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Rosella Mollicone
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2 December 2004
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105
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7
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2671-2676
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Identifiers
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