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SJ.EMBOR.7400648
SJ.EMBOR.7400648
http://dx.doi.org/10.1038/SJ.EMBOR.7400648
A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy
P356
Q24546014-B1430C9E-EF1A-42D8-B3F2-BC9FFA6399C7
P356
SJ.EMBOR.7400648
http://dx.doi.org/10.1038/SJ.EMBOR.7400648