Association of rare missense variants in the second intracellular loop of Na(V)1.7 sodium channels with familial autism

por Rubinstein, M, Patowary, A, Stanaway, I B, McCord, E, Nesbitt, R R, Archer, M, Scheuer, T, Nickerson, D, Raskind, W H, Wijsman, E M, Bernier, R, Catterall, W A, Brkanac, Z
Publicado 2018

Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders

por Truong, D. T., Shriberg, L. D., Smith, S. D., Chapman, K. L., Scheer-Cohen, A. R., DeMille, M. M. C., Adams, A. K., Nato, A. Q., Wijsman, E. M., Eicher, J. D., Gruen, J. R.
Publicado 2016