TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Wiszniewski, W; Hunter, JV; Hanchard, NA; Willer, JR; Shaw, C; Tian, Q; Illner, A; Wang, X; Cheung, SW; Patel, A; +56 more... Campbell, IM; Gelowani, V; Hixson, P; Ester, AR; Azamian, MS; Potocki, L; Zapata, G; Hernandez, PP; Ramocki, MB; Santos-Cortez, RL; Wang, G; York, MK; Justice, MJ; Chu, ZD; Bader, PI; Omo-Griffith, L; Madduri, NS; Scharer, G; Crawford, HP; Yanatatsaneejit, P; Eifert, A; Kerr, J; Bacino, CA; Franklin, AI; Goin-Kochel, RP; Simpson, G; Immken, L; Haque, ME; Stosic, M; Williams, MD; Morgan, TM; Pruthi, S; Omary, R; Boyadjiev, SA; Win, KK; Thida, A; Hurles, M; Hibberd, ML; Khor, CC; Van Vinh Chau, N; Gallagher, TE; Mutirangura, A; Stankiewicz, P; Beaudet, AL; Maletic-Savatic, M; Rosenfeld, JA; Shaffer, LG; Davis, EE; Belmont, JW; Dunstan, S; Simmons, CP; Bonnen, PE; Leal, SM; Katsanis, N; Lupski, JR; Lalani, SR; (2013) TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. American journal of human genetics, 93 (2). pp. 197-210. ISSN 0002-9297 DOI: https://doi.org/10.1016/j.ajhg.2013.05.027

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