Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism.

TitleMutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism.
Publication TypeJournal Article
AuthorsHarms, FLeonie, Girisha, KM, Hardigan, AA, Kortüm, 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-L, Drummond-Borg, M, Eldomery, MK, El-Hattab, AW, Saleh, MAM, Bézieau, S, Cogné, B, Isidor, B, Küry, S, Lupski, JR, Myers, RM, Cooper, GM, Kutsche, K
PubMed ID28017373
PubMed Central IDPMC5223027
Grant ListU54 HG006542 / HG / NHGRI NIH HHS / United States
R01 CA197139 / CA / NCI NIH HHS / United States
UM1 HG006542 / HG / NHGRI NIH HHS / United States
R21 NS094047 / NS / NINDS NIH HHS / United States
T32 GM008361 / GM / NIGMS NIH HHS / United States
UM1 HG007301 / HG / NHGRI NIH HHS / United States