A new NBIA patient from Turkey with homozygous C19ORF12 mutation.
Kasapkara ÇS, Tümer L, Gregory A, Ezgü F, İnci A, Derinkuyu BE, Fox R, Rogers C, Hayflick S.
Kasapkara ÇS, et al.
Acta Neurol Belg. 2019 Dec;119(4):623-625. doi: 10.1007/s13760-018-1026-5. Epub 2018 Oct 8.
Acta Neurol Belg. 2019.
PMID: 30298423
Free PMC article.
No abstract available.