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)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference58 articles.
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2. Congenital disorders of glycosylation: genetic model systems lead the way
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4. Killing the messenger: new insights into nonsense-mediated mRNA decay
5. Listening to silence and understanding nonsense: exonic mutations that affect splicing
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