Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B)

NRXN1 encodes thousands of splicing variants categorized into long NRXN1α, short NRXN1β and extremely short NRXN1γ, which exert differential roles in neuronal excitation/inhibition. NRXN1α deletions are common in autism spectrum disorder (ASD) and other neurodevelopmental/neuropsychiatric disorders....

תיאור מלא

מידע ביבליוגרפי

Principais autores:	Yicheng Ding, Aisling O'Brien, Berta Marcó de la Cruz, Meimei Yang, Jacqueline Fitzgerald, Guangming Yang, Weidong Li, Veronica McInerney, Janusz Krawczyk, Sally A. Lynch, Linda Howard, Nicholas M. Allen, Timothy O'Brien, Louise Gallagher, Sanbing Shen
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	Elsevier 2021-04-01
סדרה:	Stem Cell Research
גישה מקוונת:	http://www.sciencedirect.com/science/article/pii/S1873506121000684
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!