An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)
- 1 January 1994
- journal article
- case report
- Published by Hindawi Limited in Human Mutation
- Vol. 4 (1), 73-75
- https://doi.org/10.1002/humu.1380040113
Abstract
No abstract availableKeywords
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