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

Nakamura, Akikazu; Nomura, Shunsuke; Hara, Shoko; Thamamongood, Thiparpa; Maehara, Taketoshi; Nariai, Tadashi; Khairullah, Shasha; Tan, Kay Sin; Azuma, Kenko; Chida-Nagai, Ayako; Furutani, Yoshiyuki; Hori, Takahiro; Yamaguchi, Koji; Kawamata, Takakazu; Roder, Constantin; Akagawa, Hiroyuki

Publikationsdienste
→
Universitätsbibliographie
→
4 Medizinische Fakultät
→
Dokumentanzeige

« zurück

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

Autor(en):

Nakamura, Akikazu; Nomura, Shunsuke; Hara, Shoko; Thamamongood, Thiparpa; Maehara, Taketoshi; Nariai, Tadashi; Khairullah, Shasha; Tan, Kay Sin; Azuma, Kenko; Chida-Nagai, Ayako; Furutani, Yoshiyuki; Hori, Takahiro; Yamaguchi, Koji; Kawamata, Takakazu; Roder, Constantin; Akagawa, Hiroyuki

Tübinger Autor(en):

Roder, Constantin

Erschienen in:

Scientific Reports (2024), Bd. 14 (1), Article 22720

Verlagsangabe:

Berlin : Nature Portfolio

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1038/s41598-024-72043-5

ISSN:

2045-2322