Literature DB >> 19995371

Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease.

D Tsuruta1, M Akiyama, A Ishida-Yamamoto, H Imanishi, N Mizuno, J Sowa, H Kobayashi, M Ishii, I Kurokawa, H Shimizu.   

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Year:  2009        PMID： 19995371     DOI： 10.1111/j.1365-2133.2009.09580.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  3 in total

1.  A severe fatal case of Darier-White disease-an extreme phenotype or a new entity?

Authors:  Guy Shalom; Elena Kahn; Sima Halevy
Journal:  JAAD Case Rep       Date:  2015-01-12

2.  Novel and recurrent ATP2A2 mutations in Japanese patients with Darier's disease.

Authors:  Kana Noda; Takuya Takeichi; Yusuke Okuno; Hiromichi Takama; Shunsuke Miura; Shinji Kagami; Haruko Hino; Yuki Nakamura; Yumi Fujio; Izumi Konohana; Ayako Otani; Hideki Mukai; Kazumitsu Sugiura; Masashi Akiyama
Journal:  Nagoya J Med Sci       Date:  2016-12       Impact factor: 1.131

3.  Response of Human Osteoblast to n-HA/PEEK--Quantitative Proteomic Study of Bio-effects of Nano-Hydroxyapatite Composite.

Authors:  Minzhi Zhao; Haiyun Li; Xiaochen Liu; Jie Wei; Jianguo Ji; Shu Yang; Zhiyuan Hu; Shicheng Wei
Journal:  Sci Rep       Date:  2016-03-09       Impact factor: 4.379
  3 in total

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