SLC7A5 c.665-4761C>A

Variant ID: 16-87879522-G-T

NM_003486.5(SLC7A5):c.665-4761C>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A human neurodevelopmental model for Williams syndrome.

Nature
Chailangkarn, Thanathom T; Trujillo, Cleber A CA; Freitas, Beatriz C BC; Hrvoj-Mihic, Branka B; Herai, Roberto H RH; Yu, Diana X DX; Brown, Timothy T TT; Marchetto, Maria C MC; Bardy, Cedric C; McHenry, Lauren L; Stefanacci, Lisa L; Järvinen, Anna A; Searcy, Yvonne M YM; DeWitt, Michelle M; Wong, Wenny W; Lai, Philip P; Ard, M Colin MC; Hanson, Kari L KL; Romero, Sarah S; Jacobs, Bob B; Dale, Anders M AM; Dai, Li L; Korenberg, Julie R JR; Gage, Fred H FH; Bellugi, Ursula U; Halgren, Eric E; Semendeferi, Katerina K; Muotri, Alysson R AR
Publication Date: 2016-08-18

Variant appearance in text: rs997761
PubMed Link: 27509850
Variant Present in the following documents:
  • NIHMS800474-supplement-supp_info.pdf
View BVdb publication page