Mutations in NKX6-2 Cause Progressive Spastic Ataxia and HypomyelinationViorica Chelban, Henry Houlden, Nisha Patel et al.|The American Journal of Human Genetics|2017Cited by 51
Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 familiesJörn Oliver Sass, Clara van Karnebeek, Majid Alfadhel et al.|Molecular Genetics and Metabolism|2016Cited by 13
Mutations in nkx6-2 cause progressive spastic-ataxia and hypomyelinationViorica Chelban, Henry Houlden, Jana Vandrovcová et al.|Journal of the Neurological Sciences|2017Cited by 0