APA (7th ed.) Citation

Wonkam, A., Lebeko, K., Mowla, S., Noubiap, J. J., Chong, M., & Pare, G. (2021). Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon. Wiley.

Chicago Style (17th ed.) Citation

Wonkam, Ambroise, Kamogelo Lebeko, Shaheen Mowla, Jean Jacques Noubiap, Mike Chong, and Guillaume Pare. Whole Exome Sequencing Reveals a Biallelic Frameshift Mutation in GRXCR2 in Hearing Impairment in Cameroon. Wiley, 2021.

MLA (8th ed.) Citation

Wonkam, Ambroise, et al. Whole Exome Sequencing Reveals a Biallelic Frameshift Mutation in GRXCR2 in Hearing Impairment in Cameroon. Wiley, 2021.