TY  - GEN
AU  - Özgün,Nezir
AU  - Özer,Leyla
AU  - Yaramış,Ahmet
TI  - A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review
SN  - 2791-6421
PY  - 2021///0819
KW  - Carrier Proteins
KW  - genetics
KW  - Electroencephalography
KW  - Epilepsy
KW  - Female
KW  - Humans
KW  - Infant
KW  - Magnetic Resonance Imaging
KW  - Mutation
N1  - Publication Type: Case Reports; Review; Journal Article
UR  - https://doi.org/10.24953/turkjped.2020.01.015
ER  -