Chelban V et al. Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination. Am J Hum Genet. 2017;100(6):969-977. PMID: 28575651.
Dorboz I et al. Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy. Brain. 2017;140(10):2550-2556. PMID: 28969374.
Baldi C et al. Expanding the clinical and genetic spectra of NKX6-2-related disorder. Clin Genet. 2018 Feb 1. PMID: 29388673. [Epub ahead of print]
Van Haren K et al. Consensus statement on preventive and symptomatic care of leukodystrophy patients. Mol Genet Metab. 2015;114(4):516-26. PMID: 25577286.
Zhong YF et al. The dynamics of vertebrate homeobox gene evolution: gain and loss of genes in mouse and human lineages. BMC Evol Biol. 2011;11:169. PMID: 21679462.
Gehring WJ. Exploring the homeobox. Gene. 1993;135(1-2):215-21. PMID: 7903947.