Lin, Y., Wang, W., Lin, C., Zheng, Z., Fu, Q., Peng, W., & Chen, D. (2021). Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening. Orphanet Journal of Rare Diseases, 16(1), 1. https://doi.org/10.1186/s13023-021-01964-5
Chicago Style (17th ed.) CitationLin, Yiming, Wenjun Wang, Chunmei Lin, Zhenzhu Zheng, Qingliu Fu, Weilin Peng, and Dongmei Chen. "Biochemical and Molecular Features of Chinese Patients with Glutaric Acidemia Type 1 Detected Through Newborn Screening." Orphanet Journal of Rare Diseases 16, no. 1 (2021): 1. https://doi.org/10.1186/s13023-021-01964-5.
MLA (9th ed.) CitationLin, Yiming, et al. "Biochemical and Molecular Features of Chinese Patients with Glutaric Acidemia Type 1 Detected Through Newborn Screening." Orphanet Journal of Rare Diseases, vol. 16, no. 1, 2021, p. 1, https://doi.org/10.1186/s13023-021-01964-5.