A single homozygous point mutation in a 3′untranslated region motif of selenoprotein N mRNA causes SEPN1‐related myopathy
Open Access
- 24 February 2006
- journal article
- Published by Springer Nature in EMBO Reports
- Vol. 7 (4) , 450-454
Abstract
EMBO Press is an editorially independent publishing platform for the development of EMBO scientific publications.Keywords
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