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

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: 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

Creator: 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

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-024-72043-5

URN: urn:nbn:de:101:1-2412162129352.751333372011

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:29 AM CEST

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Associated

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

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Other Objects (12)

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EXCAVATOR: detecting copy number variants from whole-exome sequencing data

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