The distribution of neuroligin4, an autism-related postsynaptic molecule, in the human brain

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 due to the lack of a closely homologous gene in rod...

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Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Akie Toya, Masahide Fukada, Eiko Aoki, Tohru Matsuki, Masashi Ueda, Shima Eda, Yoshio Hashizume, Akio Iio, Shigeo Masaki, Atsuo Nakayama
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	BMC 2023-02-01
Σειρά:	Molecular Brain
Θέματα:	ASD NLGN4 Immunohistochemistry Periventricular nucleus Supraoptic nucleus Arginine-vasopressin
Διαθέσιμο Online:	https://doi.org/10.1186/s13041-023-00999-y
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