(Q28258466)

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An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id)

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An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id) (English)

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congenital disorder

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congenital disorder

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congenital disorder of glycosylation

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author name string

Jonas Denecke

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Christian Kranz

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Dirk Kemming

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Hans-Georg Koch

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Thorsten Marquardt

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language of work or name

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publication date

May 2004

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23

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477-86

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5

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Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance

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Identifiers

10.1002/HUMU.20026

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