Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene.

MLA

Souissi, Amal, et al. “Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 Gene.” Genetic Testing and Molecular Biomarkers, vol. 25, no. 8, Aug. 2021, pp. 528–39. EBSCOhost, https://doi.org/10.1089/gtmb.2021.0092.

APA

Souissi, A., Ben Said, M., Frikha, F., Elloumi, I., Masmoudi, S., & Megarbane, A. (2021). Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene. Genetic Testing and Molecular Biomarkers, 25(8), 528–539. https://doi.org/10.1089/gtmb.2021.0092

Chicago

Souissi, Amal, Mariem Ben Said, Fakher Frikha, Ines Elloumi, Saber Masmoudi, and Andre Megarbane. 2021. “Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 Gene.” Genetic Testing and Molecular Biomarkers 25 (8): 528–39. doi:10.1089/gtmb.2021.0092.