De novo occurrence of the filaggrin mutation p.R501X with prevalent mutation c.3321delA in a Japanese family with ichthyosis vulgaris complicated by atopic dermatitis.

MLA

Hamada, Takahiro, et al. “De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic Dermatitis.” The Journal of Investigative Dermatology, vol. 128, no. 5, May 2008, pp. 1323–25. EBSCOhost, https://doi.org/10.1038/sj.jid.5701164.

APA

Hamada, T., Sandilands, A., Fukuda, S., Sakaguchi, S., Ohyama, B., Yasumoto, S., McLean, W. H. I., & Hashimoto, T. (2008). De novo occurrence of the filaggrin mutation p.R501X with prevalent mutation c.3321delA in a Japanese family with ichthyosis vulgaris complicated by atopic dermatitis. The Journal of Investigative Dermatology, 128(5), 1323–1325. https://doi.org/10.1038/sj.jid.5701164

Chicago

Hamada, Takahiro, Aileen Sandilands, Shunpei Fukuda, Sachiko Sakaguchi, Bungo Ohyama, Shinichiro Yasumoto, W H Irwin McLean, and Takashi Hashimoto. 2008. “De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic Dermatitis.” The Journal of Investigative Dermatology 128 (5): 1323–25. doi:10.1038/sj.jid.5701164.