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Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome.

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Bibliographic Details
Title: Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome.
Authors: Nakamura, Akikazu1,2 (AUTHOR), Nomura, Shunsuke3,4 (AUTHOR), Hara, Shoko5 (AUTHOR), Thamamongood, Thiparpa5 (AUTHOR), Maehara, Taketoshi5 (AUTHOR), Nariai, Tadashi5 (AUTHOR), Khairullah, Shasha6 (AUTHOR), Tan, Kay Sin7 (AUTHOR), Azuma, Kenko1 (AUTHOR), Chida‐Nagai, Ayako8,9 (AUTHOR), Furutani, Yoshiyuki9 (AUTHOR), Hori, Takahiro1,2 (AUTHOR), Yamaguchi, Koji2 (AUTHOR), Kawamata, Takakazu2 (AUTHOR), Roder, Constantin10 (AUTHOR), Akagawa, Hiroyuki1,11,12 (AUTHOR) akagawa.hiroyuki@twmu.ac.jp
Source: Scientific Reports. 10/4/2024, Vol. 14 Issue 1, p1-13. 13p.
Database: Academic Search Ultimate
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Description
ISSN:20452322
DOI:10.1038/s41598-024-72043-5