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Literature for DOID 450: myotonic disease
Xenbase Articles
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Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia.,
Meyer-Kleine C,Steinmeyer K,Ricker K,Jentsch TJ,Koch MC,
Am J Hum Genet. December 1, 1995; 57(6):1537-6605.
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