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31. Mutation analyses of patients with dyschromatosis symmetrica hereditaria: Ten novel mutations of the ADAR1 gene. Issue 1 (July 2015)

33. NGS‐based targeted resequencing identified rare subtypes of albinism: Providing accurate molecular diagnosis for Japanese patients with albinism. (9th June 2019)

35. Novel AP3B1 compound heterozygous mutations in a Japanese patient with Hermansky–Pudlak syndrome type 2. Issue 2 (9th December 2019)

36. Novel AP3B1 mutations in a Hermansky–Pudlak syndrome type2 with neonatal interstitial lung disease. Issue 2 (21st February 2022)

37. Novel imaging and quantification methods for the evaluation of disease severity in vitiligo and chemical leukoderma. Issue 2 (May 2017)