A mutation in the SEPN1 selenocysteine redefinition element...

Human Mutation 2009 Vol. 30; Iss. 3

A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy

Baijayanta Maiti, Sandrine Arbogast, Valérie Allamand, Mark W. Moyle, Christine B. Anderson, Pascale Richard, Pascale Guicheney, Ana Ferreiro, Kevin M. Flanigan, Michael T. Howard
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Volume:
30
Year:
2009
Language:
english
Pages:
6
DOI:
10.1002/humu.20879
File:
PDF, 226 KB
english, 2009
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