YILMAZ, B. Et Al. 2015. Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.. Journal of pediatric endocrinology & metabolism : JPEM , vol.28 , 1179-81.

YILMAZ, B., KOR, D., Mungan, N., ERDEM, S., & CEYLANER, S., (2015). Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.. Journal of pediatric endocrinology & metabolism : JPEM , vol.28, 1179-81.

YILMAZ, BİLGE Et Al. "Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.," Journal of pediatric endocrinology & metabolism : JPEM , vol.28, 1179-81, 2015

YILMAZ, BİLGE Et Al. "Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.." Journal of pediatric endocrinology & metabolism : JPEM , vol.28, pp.1179-81, 2015

YILMAZ, B. Et Al. (2015) . "Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.." Journal of pediatric endocrinology & metabolism : JPEM , vol.28, pp.1179-81.

@article{article, author={BİLGE YILMAZ Et Al. }, title={Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.}, journal={Journal of pediatric endocrinology & metabolism : JPEM}, year=2015, pages={1179-81} }