İNCİ, A. Et Al. 2022. An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation. NEUROLOGY ASIA , vol.27, no.1 , 199-202.

İNCİ, A., OKUR, İ., DEMİR, E., BİBEROĞLU, G., TÜMER, L., SERDAROĞLU, A., ... EZGÜ, F. S.(2022). An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation. NEUROLOGY ASIA , vol.27, no.1, 199-202.

İNCİ, ASLI Et Al. "An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation," NEUROLOGY ASIA , vol.27, no.1, 199-202, 2022

İNCİ, ASLI Et Al. "An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation." NEUROLOGY ASIA , vol.27, no.1, pp.199-202, 2022

İNCİ, A. Et Al. (2022) . "An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation." NEUROLOGY ASIA , vol.27, no.1, pp.199-202.

@article{article, author={ASLI İNCİ Et Al. }, title={An ultra-rare cause of severe hypotonia mimicking Pompe disease in an infant: RRM2B related mitochon- drial DNA depletion syndrome with a novel mutation}, journal={NEUROLOGY ASIA}, year=2022, pages={199-202} }