PARILTAY, E. Et Al. 2022. A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report. CLINICAL NEUROLOGY AND NEUROSURGERY , vol.212 .

PARILTAY, E., PARILTAY, E., TALİM, B., & Onay, H., (2022). A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report. CLINICAL NEUROLOGY AND NEUROSURGERY , vol.212.

PARILTAY, ERHAN Et Al. "A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report," CLINICAL NEUROLOGY AND NEUROSURGERY , vol.212, 2022

PARILTAY, ERHAN Et Al. "A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report." CLINICAL NEUROLOGY AND NEUROSURGERY , vol.212, 2022

PARILTAY, E. Et Al. (2022) . "A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report." CLINICAL NEUROLOGY AND NEUROSURGERY , vol.212.

@article{article, author={ERHAN PARILTAY Et Al. }, title={A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report}, journal={CLINICAL NEUROLOGY AND NEUROSURGERY}, year=2022}