Cita APA

R, U., E, L., A, M., M, P., L, C., LA, P., . . . S, B. (2020). Five new cases of syndromic intellectual disability due to KAT6A mutations: Widening the molecular and clinical spectrum.

Citación estilo Chicago

R, Urreizti, et al. Five New Cases of Syndromic Intellectual Disability Due to KAT6A Mutations: Widening the Molecular and Clinical Spectrum. 2020.

Cita MLA

R, Urreizti, et al. Five New Cases of Syndromic Intellectual Disability Due to KAT6A Mutations: Widening the Molecular and Clinical Spectrum. 2020.