Information Journal Paper
APA:
Copy. (2019). A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin. BMC MEDICAL GENETICS, 20(1), 0-0. SID. https://sid.ir/paper/776455/en
Vancouver:
Copy. A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin. BMC MEDICAL GENETICS[Internet]. 2019;20(1):0-0. Available from: https://sid.ir/paper/776455/en
IEEE:
Copy, “A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin,” BMC MEDICAL GENETICS, vol. 20, no. 1, pp. 0–0, 2019, [Online]. Available: https://sid.ir/paper/776455/en