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Mutations in EBF3 disturb transcriptional profiles and underlie a novel syndrome of intellectual disability, ataxia and facial dysmorphism, Harms, FL;Girisha, KM;Hardigan, VO;Kortum, F;Shukla, A;Alawi, M;Dalal, A;Brady, L;Tarnopolsky, M;Bird, LM;Ceulemans, S;Bebin, M;Bowling, KM;Hiatt, SM;Lose, EJ;Primiano, M;Chung, WK;Juusola, J;Akdemir, ZC;Bainbridge, M;Charng, W;Drummond-Borg, M;Eldomery, MK;El-Hattab, AW;Saleh, MA;Bezieau, S;Cogne, B;Isidor, B;Kury, S;Lupski, JR;Myers, RM;Cooper, GM;Kutsche, K;, bioRxiv 2016 PS100010

 

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