Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms
- 1 March 1991
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 86 (5) , 457-462
- https://doi.org/10.1007/bf00194633
Abstract
No abstract availableKeywords
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