Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome ; volume:14 ; number:1 ; day:4 ; month:10 ; year:2024 ; pages:1-13 ; date:12.2024
Scientific reports ; 14, Heft 1 (4.10.2024), 1-13, 12.2024
- Urheber
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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
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41598-024-72043-5
- URN
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urn:nbn:de:101:1-2412162129352.751333372011
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:29 MESZ
Datenpartner
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Beteiligte
- 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
- SpringerLink (Online service)
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