Ascari, G., Peelman, F., Farinelli, P., Rosseel, T., Lambrechts, N., Wunderlich, K. A., . . . Coppieters, F. (2020). Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility. Hum Mutat.
Style de citation ChicagoAscari, Giulia, et al. "Functional Characterization of the First Missense Variant in CEP78, a Founder Allele Associated With Cone‐rod Dystrophy, Hearing Loss, and Reduced Male Fertility." Hum Mutat 2020.
Style de citation MLAAscari, Giulia, et al. "Functional Characterization of the First Missense Variant in CEP78, a Founder Allele Associated With Cone‐rod Dystrophy, Hearing Loss, and Reduced Male Fertility." Hum Mutat 2020.
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