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Showing results 9 to 11 of 11

Issue DateTitleAuthor(s)Type
2016First identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy박형준Letter
2015Molecular genetic diagnosis of a bethlem myopathy family with an autosomal-dominant COL6A1 mutation, as evidenced by exome sequencing박형준Article
2014The role of insulin resistance in diabetic neuropathy in Koreans with type 2 diabetes mellitus: A 6-year follow-up study박형준Article
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