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Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients.
Maezawa Y, Kato H, Takemoto M, Watanabe A, Koshizaka M, Ishikawa T, Sargolzaeiaval F, Kuzuya M, Wakabayashi H, Kusaka T, Yokote K, Oshima J. Maezawa Y, et al. Among authors: sargolzaeiaval f. Mol Syndromol. 2018 Jul;9(4):214-218. doi: 10.1159/000489055. Epub 2018 May 15. Mol Syndromol. 2018. PMID: 30140198 Free PMC article.