YILDIRIM, M. Et Al. 2021. Mild congenital myopathy due to a novel variation in SPEG gene. INTRACTABLE & RARE DISEASES RESEARCH , vol.10, no.3 , 220-222.

YILDIRIM, M., Balasar, O., KÖSE, E., & Dogan, M. T., (2021). Mild congenital myopathy due to a novel variation in SPEG gene. INTRACTABLE & RARE DISEASES RESEARCH , vol.10, no.3, 220-222.

YILDIRIM, MİRAÇ Et Al. "Mild congenital myopathy due to a novel variation in SPEG gene," INTRACTABLE & RARE DISEASES RESEARCH , vol.10, no.3, 220-222, 2021

YILDIRIM, MİRAÇ Et Al. "Mild congenital myopathy due to a novel variation in SPEG gene." INTRACTABLE & RARE DISEASES RESEARCH , vol.10, no.3, pp.220-222, 2021

YILDIRIM, M. Et Al. (2021) . "Mild congenital myopathy due to a novel variation in SPEG gene." INTRACTABLE & RARE DISEASES RESEARCH , vol.10, no.3, pp.220-222.

@article{article, author={MİRAÇ YILDIRIM Et Al. }, title={Mild congenital myopathy due to a novel variation in SPEG gene}, journal={INTRACTABLE & RARE DISEASES RESEARCH}, year=2021, pages={220-222} }