Merkoša sitáhtat
APA-čujuhus (7. p.)
Geng, J., Sun, Y., Zhao, Y., Xiong, W., Zhong, M., Zhang, Y., . . . Yuan, H. (2021). Two novel BTD mutations causing profound biotinidase deficiency in a Chinese patient. Wiley.
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Chicago-čujuhus (17. p.)
Geng, Jia, et al. Two Novel BTD Mutations Causing Profound Biotinidase Deficiency in a Chinese Patient. Wiley, 2021.
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MLA-čujuhus (9. p.)
Geng, Jia, et al. Two Novel BTD Mutations Causing Profound Biotinidase Deficiency in a Chinese Patient. Wiley, 2021.
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