APA (7th ed.) Citation

Zastrow, D. B., Baudet, H., Shen, W., Thomas, A., Si, Y., Weaver, M. A., . . . Mao, R. (2018). Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the phenylalanine hydroxylase gene. Human mutation, 39(11), . https://doi.org/10.1002/humu.23649

Chicago Style (17th ed.) Citation

Zastrow, Diane B., et al. "Unique Aspects of Sequence Variant Interpretation for Inborn Errors of Metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene." Human Mutation 39, no. 11 (2018). https://doi.org/10.1002/humu.23649.

MLA (9th ed.) Citation

Zastrow, Diane B., et al. "Unique Aspects of Sequence Variant Interpretation for Inborn Errors of Metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene." Human Mutation, vol. 39, no. 11, 2018, https://doi.org/10.1002/humu.23649.