Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder ; volume:28 ; number:10 ; day:30 ; month:5 ; year:2023 ; pages:4294-4306 ; date:10.2023
Molecular psychiatry ; 28, Heft 10 (30.5.2023), 4294-4306, 10.2023

Creator: Nishioka, Masaki
Takayama, Jun
Sakai, Naomi
Kazuno, An-a
Ishiwata, Mizuho
Ueda, Junko
Hayama, Takashi
Fujii, Kumiko
Someya, Toshiyuki
Kuriyama, Shinichi
Tamiya, Gen
Takata, Atsushi
Kato, Tadafumi

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41380-023-02096-x

URN: urn:nbn:de:101:1-2024041012063478225470

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

Last update: 14.08.2025, 10:58 AM CEST

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Nishioka, Masaki
Takayama, Jun
Sakai, Naomi
Kazuno, An-a
Ishiwata, Mizuho
Ueda, Junko
Hayama, Takashi
Fujii, Kumiko
Someya, Toshiyuki
Kuriyama, Shinichi
Tamiya, Gen
Takata, Atsushi
Kato, Tadafumi
SpringerLink (Online service)

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Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder

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Other Objects (12)

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PACS1-Neurodevelopmental disorder: clinical features and trial readiness

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Investigating the impact of the environment on neurodevelopmental disorder

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STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics

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Neurodevelopmental profile of Fetal Alcohol Spectrum Disorder: A systematic review

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Further delineation of the SCAF4-associated neurodevelopmental disorder

PACS1-Neurodevelopmental disorder: clinical features and trial readiness

Exome Pool-Seq in neurodevelopmental disorders

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

Investigating the impact of the environment on neurodevelopmental disorder

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STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics

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Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

Neurodevelopmental profile of Fetal Alcohol Spectrum Disorder: A systematic review

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