A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss.

MLA

Ullah, Farid, et al. “A Recessive Variant in TFAM Causes MtDNA Depletion Associated with Primary Ovarian Insufficiency, Seizures, Intellectual Disability and Hearing Loss.” Human Genetics, vol. 140, no. 12, Dec. 2021, pp. 1733–51. EBSCOhost, https://doi.org/10.1007/s00439-021-02380-2.

APA

Ullah, F., Rauf, W., Khan, K., Khan, S., Bell, K. M., de Oliveira, V. C., Tariq, M., Bakhshalizadeh, S., Touraine, P., Katsanis, N., Sinclair, A., He, S., Tucker, E. J., Baig, S. M., & Davis, E. E. (2021). A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss. Human Genetics, 140(12), 1733–1751. https://doi.org/10.1007/s00439-021-02380-2

Chicago

Ullah, Farid, Waqar Rauf, Kamal Khan, Sheraz Khan, Katrina M Bell, Vanessa Cristina de Oliveira, Muhammad Tariq, et al. 2021. “A Recessive Variant in TFAM Causes MtDNA Depletion Associated with Primary Ovarian Insufficiency, Seizures, Intellectual Disability and Hearing Loss.” Human Genetics 140 (12): 1733–51. doi:10.1007/s00439-021-02380-2.