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A new NBIA patient from Turkey with homozygous C19ORF12 mutation
Kasapkara, Çiğdem Seher, Tümer, Leyla, Gregory, Allison, Ezgü, Fatih, İnci, Aslı, Derinkuyu, Betül Emine, Fox, Rachel, Rogers, Caleb, Hayflick, SusanLanguage:
english
Journal:
Acta Neurologica Belgica
DOI:
10.1007/s13760-018-1026-5
Date:
October, 2018
File:
PDF, 731 KB
english, 2018