Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency.
Nogueira C, Barros J, Sá MJ, Azevedo L, Taipa R, Torraco A, Meschini MC, Verrigni D, Nesti C, Rizza T, Teixeira J, Carrozzo R, Pires MM, Vilarinho L, Santorelli FM.
Nogueira C, et al. Among authors: taipa r.
Neurogenetics. 2013 May;14(2):153-60. doi: 10.1007/s10048-013-0361-1. Epub 2013 Mar 28.
Neurogenetics. 2013.
PMID: 23532514