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3. Atypical presentation of infantile‐onset farber disease with novel ASAH1 mutations. Issue 11 (13th July 2016)

5. Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center. Issue 5 (20th January 2017)

6. Importance of early diagnosis in LMNA‐related muscular dystrophy for cardiac surveillance. Issue 6 (30th September 2019)