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23. 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 Acta Neurol Belg; 2019 Dec; 119(4):623-625. PubMed ID: 30298423 [No Abstract] [Full Text] [Related]
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