A case of Björnstad syndrome caused by novel compound heterozygous mutations in theBCS1Lgene

MLA

Yoshiyuki Kawamoto, et al. “A Case of Björnstad Syndrome Caused by Novel Compound Heterozygous Mutations in TheBCS1Lgene.” British Journal of Dermatology, vol. 170, Apr. 2014, pp. 970–73. EBSCOhost, https://doi.org/10.1111/bjd.12736.

APA

Yoshiyuki Kawamoto, Takeshi Yanagishita, Nobuhiko Taguchi, Kazumitsu Sugiura, Masashi Akiyama, Yuki Marubashi, Keiko Ito, & Daisuke Watanabe. (2014). A case of Björnstad syndrome caused by novel compound heterozygous mutations in theBCS1Lgene. British Journal of Dermatology, 170, 970–973. https://doi.org/10.1111/bjd.12736

Chicago

Yoshiyuki Kawamoto, Takeshi Yanagishita, Nobuhiko Taguchi, Kazumitsu Sugiura, Masashi Akiyama, Yuki Marubashi, Keiko Ito, and Daisuke Watanabe. 2014. “A Case of Björnstad Syndrome Caused by Novel Compound Heterozygous Mutations in TheBCS1Lgene.” British Journal of Dermatology 170 (April): 970–73. doi:10.1111/bjd.12736.