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Nakamura, Akikazu and Nomura, Shunsuke and Hara, Shoko and Thamamongood, Thiparpa and Maehara, Taketoshi and Nariai, Tadashi and Khairullah, Shasha and Tan, Kay Sin and Azuma, Kenko and Chida-Nagai, Ayako and Furutani, Yoshiyuki and Hori, Takahiro and Yamaguchi, Koji and Kawamata, Takakazu and Roder, Constantin and Akagawa, Hiroyuki (2024) Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome. Scientific Reports, 14 (1). ISSN 2045-2322, DOI https://doi.org/10.1038/s41598-024-72043-5.
