Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Akie Toya"'
Autor:
Akie Toya, Masahide Fukada, Eiko Aoki, Tohru Matsuki, Masashi Ueda, Shima Eda, Yoshio Hashizume, Akio Iio, Shigeo Masaki, Atsuo Nakayama
Publikováno v:
Molecular Brain, Vol 16, Iss 1, Pp 1-14 (2023)
Abstract NLGN4X was identified as a single causative gene of rare familial nonsyndromic autism for the first time. It encodes the postsynaptic membrane protein Neuroligin4 (NLGN4), the functions and roles of which, however, are not fully understood d
Externí odkaz:
https://doaj.org/article/64f35ca121e6410dbeece3b4d1bc9c46
Autor:
Masashi Ueda, Tohru Matsuki, Masahide Fukada, Shima Eda, Akie Toya, Akio Iio, Hidenori Tabata, Atsuo Nakayama
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Zhu-Tokita-Takenouchi-Kim (ZTTK) syndrome, a rare congenital anomaly syndrome characterized by intellectual disability, brain malformation, facial dysmorphism, musculoskeletal abnormalities, and some visceral malformations is caused by de no
Externí odkaz:
https://doaj.org/article/407a176e363f46fca3b22304b6db3edc
Autor:
Masashi Ueda, Tohru Matsuki, Masahide Fukada, Shima Eda, Akie Toya, Akio Iio, Hidenori Tabata, Atsuo Nakayama
Zhu-Tokita-Takenouchi-Kim (ZTTK) syndrome, a rare congenital anomaly syndrome characterized by intellectual disability, brain malformation, facial dysmorphism, musculoskeletal abnormalities, and some visceral malformations is caused by de novo hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e56334cf673025ae297e3864f87a106b
https://doi.org/10.21203/rs.3.rs-17672/v1
https://doi.org/10.21203/rs.3.rs-17672/v1
