ATM c.1089del ;(p.L364Wfs*26)

Variant ID: 11-108119681-TC-T

NM_000051.3(ATM):c.1089del;(p.L364Wfs*26)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.

Journal Of Medical Genetics
Platzer, Konrad K; Yuan, Hongjie H; Schütz, Hannah H; Winschel, Alexander A; Chen, Wenjuan W; Hu, Chun C; Kusumoto, Hirofumi H; Heyne, Henrike O HO; Helbig, Katherine L KL; Tang, Sha S; Willing, Marcia C MC; Tinkle, Brad T BT; Adams, Darius J DJ; Depienne, Christel C; Keren, Boris B; Mignot, Cyril C; Frengen, Eirik E; Strømme, Petter P; Biskup, Saskia S; Döcker, Dennis D; Strom, Tim M TM; Mefford, Heather C HC; Myers, Candace T CT; Muir, Alison M AM; LaCroix, Amy A; Sadleir, Lynette L; Scheffer, Ingrid E IE; Brilstra, Eva E; van Haelst, Mieke M MM; van der Smagt, Jasper J JJ; Bok, Levinus A LA; Møller, Rikke S RS; Jensen, Uffe B UB; Millichap, John J JJ; Berg, Anne T AT; Goldberg, Ethan M EM; De Bie, Isabelle I; Fox, Stephanie S; Major, Philippe P; Jones, Julie R JR; Zackai, Elaine H EH; Abou Jamra, Rami R; Rolfs, Arndt A; Leventer, Richard J RJ; Lawson, John A JA; Roscioli, Tony T; Jansen, Floor E FE; Ranza, Emmanuelle E; Korff, Christian M CM; Lehesjoki, Anna-Elina AE; Courage, Carolina C; Linnankivi, Tarja T; Smith, Douglas R DR; Stanley, Christine C; Mintz, Mark M; McKnight, Dianalee D; Decker, Amy A; Tan, Wen-Hann WH; Tarnopolsky, Mark A MA; Brady, Lauren I LI; Wolff, Markus M; Dondit, Lutz L; Pedro, Helio F HF; Parisotto, Sarah E SE; Jones, Kelly L KL; Patel, Anup D AD; Franz, David N DN; Vanzo, Rena R; Marco, Elysa E; Ranells, Judith D JD; Di Donato, Nataliya N; Dobyns, William B WB; Laube, Bodo B; Traynelis, Stephen F SF; Lemke, Johannes R JR
Publication Date: 2017-07

Variant appearance in text: ATD: 1088del
PubMed Link: 28377535
Variant Present in the following documents:
  • Main text
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