TY  - GEN
AU  - Kasapkara,Çiğdem Seher
AU  - Tümer,Leyla
AU  - Gregory,Allison
AU  - Ezgü,Fatih
AU  - İnci,Aslı
AU  - Derinkuyu,Betül Emine
AU  - Fox,Rachel
AU  - Rogers,Caleb
AU  - Hayflick,Susan
TI  - A new NBIA patient from Turkey with homozygous C19ORF12 mutation
SN  - 2240-2993
PY  - 2020///0406
KW  - Homozygote
KW  - Humans
KW  - Iron Metabolism Disorders
KW  - genetics
KW  - Mitochondrial Proteins
KW  - Mutation
KW  - Neuroaxonal Dystrophies
KW  - Turkey
N1  - Publication Type: Case Reports; Letter
UR  - https://doi.org/10.1007/s13760-018-1026-5
ER  -