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8. Dorboz, Imen, Aiello, Chiara, Simons, Cas, Rodriguez, Diana, Bertini, Enrico. . Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy. In Brain : a journal of neurology, 140, 2550-2556. doi:10.1093/brain/awx207. https://pubmed.ncbi.nlm.nih.gov/28969374/
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