Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes
De novo mutations significantly contribute to autism spectrum disorders (ASD). Here, the authors demonstrate that ASD-associated de novo mutations in the POGZ gene, one of a high-confidence ASD gene, lead to ASD-related impaired neuronal development and disrupted mature cortical network function.
Saved in:
Main Authors: | Kensuke Matsumura, Kaoru Seiriki, Shota Okada, Masashi Nagase, Shinya Ayabe, Ikuko Yamada, Tamio Furuse, Hirotoshi Shibuya, Yuka Yasuda, Hidenaga Yamamori, Michiko Fujimoto, Kazuki Nagayasu, Kana Yamamoto, Kohei Kitagawa, Hiroki Miura, Nanaka Gotoda-Nishimura, Hisato Igarashi, Misuzu Hayashida, Masayuki Baba, Momoka Kondo, Shigeru Hasebe, Kosei Ueshima, Atsushi Kasai, Yukio Ago, Atsuko Hayata-Takano, Norihito Shintani, Tokuichi Iguchi, Makoto Sato, Shun Yamaguchi, Masaru Tamura, Shigeharu Wakana, Atsushi Yoshiki, Ayako M. Watabe, Hideyuki Okano, Kazuhiro Takuma, Ryota Hashimoto, Hitoshi Hashimoto, Takanobu Nakazawa |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2020
|
Subjects: | |
Online Access: | https://doaj.org/article/b3970c6881ab49c4a520b80ed0ce7f6e |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
by: Reut Suliman-Lavie, et al.
Published: (2020) -
Author Correction: Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
by: Reut Suliman-Lavie, et al.
Published: (2021) -
Empirical Rule of Stiction of Suction Cup
by: Mitsuo Matsuda, et al.
Published: (2008) -
Altered sulcogyral patterns of orbitofrontal cortex in a large cohort of patients with schizophrenia
by: Shuichi Isomura, et al.
Published: (2017) -
Exploring rare cellular activity in more than one million cells by a transscale scope
by: T. Ichimura, et al.
Published: (2021)