Search Results - Tomonari Awaya

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    Noniron deficiency microcytic anemia, dysmorphic features, and intellectual disability: Diagnostic clues for α-thalassemia/mental retardation associated with chromosome 16 syndrome... by Kentaro Tamura, Tomonari Awaya, Takahito Wada, Tatsuya Fujii, Taketoshi Yoshida

    Published 2022
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    Branchpoints as potential targets of exon-skipping therapies for genetic disorders by Hiroaki Ohara, Motoyasu Hosokawa, Tomonari Awaya, Atsuko Hagiwara, Ryo Kurosawa, Yukiya Sako, Megumu Ogawa, Masashi Ogasawara, Satoru Noguchi, Yuichi Goto, Ryosuke Takahashi, Ichizo Nishino, Masatoshi Hagiwara

    Published 2023
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