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A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen disease

Kishore R Kumar1, Karl Ng, Himesha Vandebona

  • 1Department of Neurology, Royal North Shore Hospital and University of Sydney, St. Leonards, New South Wales 2065, Australia.

Muscle & Nerve
|February 2, 2010
PubMed

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