Kilic, M. Et Al. 2020. Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.182, is.7 , 1608-1614.

Kilic, M., Dorum, S., Topak, A., Yazici, M. U. , EZGÜ, F. S. , & COŞKUN, T., (2020). Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.182, is.7, 1608-1614.

Kilic, Mustafa Et Al. "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.182, is.7, 1608-1614, 2020

Kilic, Mustafa Et Al. "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.182, is.7, pp.1608-1614, 2020

Kilic, M. Et Al. (2020) . "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.182, is.7, pp.1608-1614.

@article{article, author={Mustafa Kilic Et Al. }, title={Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2020, pages={1608-1614} }