Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy

Imen Dorboz, Chiara Aiello, Cas Simons, Robert Thompson Stone, Marcello Niceta, Monique Elmaleh, Mohammad Abuawad, Diane Doummar, Alessandro Bruselles, Nicole I. Wolf, Lorena Travaglini, Odile Boespflug-Tanguy, Marco Tartaglia, Adeline Vanderver, Diana Rodriguez, Enrico Bertini

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)2550-2556
JournalBrain
Volume140
DOIs
Publication statusPublished - Oct 2017

Cite this

Dorboz, I., Aiello, C., Simons, C., Stone, R. T., Niceta, M., Elmaleh, M., ... Bertini, E. (2017). Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy. Brain, 140, 2550-2556. https://doi.org/10.1093/brain/awx215