Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of kitamura, a clinical entity distinct from dowling-degos disease

Michihiro Kono, Kazumitsu Sugiura, Mutsumi Suganuma, Masahiro Hayashi, Hiromichi Takama, Tamio Suzuki, UKayoko Matsunaga, Yasushi Tomita, Masashi Akiyama

Research output: Contribution to journalArticlepeer-review

26 Citations (Scopus)

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