Citations for
1CMT2O, DYNC1H1
Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease.
Weedon MN, Hastings R, Caswell R, Xie W, Paszkiewicz K, Antoniadi T, Williams M, King C, Greenhalgh L, Newbury-Ecob R, Ellard S.
Am J Hum Genet 89(2):308-12. doi: 10.1016/j.ajhg.2011.07.002. Epub 2011 Aug 4. 2011