Novel PTCH1 mutations in Japanese familial nevoid basal cell carcinoma syndrome

MLA

Tetsuya Yamamoto, et al. “Novel PTCH1 Mutations in Japanese Familial Nevoid Basal Cell Carcinoma Syndrome.” Human Genome Variation, vol. 7, Nov. 2020. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....05fb62193a84cd8e8511854ea35433b9&authtype=sso&custid=ns315887.

APA

Tetsuya Yamamoto, Shigeaki Toratani, Yoji Nakase, Naoya Kitamura, Atsuko Hamada, Tsuyoshi Hata, & Tetsuji Okamoto. (2020). Novel PTCH1 mutations in Japanese familial nevoid basal cell carcinoma syndrome. Human Genome Variation, 7.

Chicago

Tetsuya Yamamoto, Shigeaki Toratani, Yoji Nakase, Naoya Kitamura, Atsuko Hamada, Tsuyoshi Hata, and Tetsuji Okamoto. 2020. “Novel PTCH1 Mutations in Japanese Familial Nevoid Basal Cell Carcinoma Syndrome.” Human Genome Variation 7 (November). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....05fb62193a84cd8e8511854ea35433b9&authtype=sso&custid=ns315887.