Yuta Araki
3PUBLICATIONS
18CO-AUTHORS
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Publications (3)
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|Nov 06, 2020
Report of two Japanese patients with piebaldism including a novel mutation in KIT.Kei Nagatani, Ken Okamura, Kazumoto Katagiri
|Sep 27, 2020
Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families.Yuta Araki, Ken Okamura, Toru Saito
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Frequent Collaborators
3 joint publications
Ken Okamura
1 joint publications
Kazuhiko Matsumoto
1 joint publications
Ken Natsuga
1 joint publications
Yaei Togawa
1 joint publications
Tamio Suzuki
1 joint publications
Kei Nagatani
1 joint publications
Chikako Nishigori
1 joint publications
Toru Saito
1 joint publications
Atsushi Tanemura
1 joint publications
Naoki Oiso