Youssefian, L., Touati, A., Saeidian, A. H., Zargari, O., Zeinali, S., Vahidnezhad, H., & Uitto, J. (2017). A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome. Orphanet J Rare Dis.
シカゴスタイル引用形Youssefian, Leila, Andrew Touati, Amir Hossein Saeidian, Omid Zargari, Sirous Zeinali, Hassan Vahidnezhad, , Jouni Uitto. "A Novel Mutation in ST14 At a Functionally Significant Amino Acid Residue Expands the Spectrum of Ichthyosis-hypotrichosis Syndrome." Orphanet J Rare Dis 2017.
MLA引用形式Youssefian, Leila, et al. "A Novel Mutation in ST14 At a Functionally Significant Amino Acid Residue Expands the Spectrum of Ichthyosis-hypotrichosis Syndrome." Orphanet J Rare Dis 2017.