ADA c.976A>G ;(p.N326D)

Variant ID: 20-43249042-T-C

NM_000022.2(ADA):c.976A>G;(p.N326D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans.

Blood
Candotti, Fabio F; Shaw, Kit L KL; Muul, Linda L; Carbonaro, Denise D; Sokolic, Robert R; Choi, Christopher C; Schurman, Shepherd H SH; Garabedian, Elizabeth E; Kesserwan, Chimene C; Jagadeesh, G Jayashree GJ; Fu, Pei-Yu PY; Gschweng, Eric E; Cooper, Aaron A; Tisdale, John F JF; Weinberg, Kenneth I KI; Crooks, Gay M GM; Kapoor, Neena N; Shah, Ami A; Abdel-Azim, Hisham H; Yu, Xiao-Jin XJ; Smogorzewska, Monika M; Wayne, Alan S AS; Rosenblatt, Howard M HM; Davis, Carla M CM; Hanson, Celine C; Rishi, Radha G RG; Wang, Xiaoyan X; Gjertson, David D; Yang, Otto O OO; Balamurugan, Arumugam A; Bauer, Gerhard G; Ireland, Joanna A JA; Engel, Barbara C BC; Podsakoff, Gregory M GM; Hershfield, Michael S MS; Blaese, R Michael RM; Parkman, Robertson R; Kohn, Donald B DB
Publication Date: 2012-11-01

Variant appearance in text: ADA: 976A>G
PubMed Link: 22968453
Variant Present in the following documents:
  • Main text
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