B. S. Yilmaz Et Al. , "Primary systemic carnitine deficiency: A Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up," Journal of Pediatric Endocrinology and Metabolism , vol.28, no.9-10, pp.1179-1181, 2015
Yilmaz, B. S. 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 and Metabolism , vol.28, no.9-10 , 1179-1181.
Yilmaz, B. S., KOR, D., Mungan, N. O., 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 and Metabolism , vol.28, no.9-10, 1179-1181.
Yilmaz, Berna Et Al. "Primary systemic carnitine deficiency: A Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up," Journal of Pediatric Endocrinology and Metabolism , vol.28, no.9-10, 1179-1181, 2015
Yilmaz, Berna S. Et Al. "Primary systemic carnitine deficiency: A Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up." Journal of Pediatric Endocrinology and Metabolism , vol.28, no.9-10, pp.1179-1181, 2015
Yilmaz, B. S. 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 and Metabolism , vol.28, no.9-10, pp.1179-1181.
@article{article, author={Berna Seker 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 and Metabolism}, year=2015, pages={1179-1181} }