Urreizti, R., López-Martin, E., Martínez-Monseny, A., Pujadas, M., Castilla-Vallmanya, L., Pérez-Jurado, L. A., . . . Balcells Comas, S. (2020). Five new cases of syndromic intellectual disability due to KAT6A mutations: Widening the molecular and clinical spectrum.
Citación estilo ChicagoUrreizti, Roser, et al. Five New Cases of Syndromic Intellectual Disability Due to KAT6A Mutations: Widening the Molecular and Clinical Spectrum. 2020.
Cita MLAUrreizti, Roser, et al. Five New Cases of Syndromic Intellectual Disability Due to KAT6A Mutations: Widening the Molecular and Clinical Spectrum. 2020.
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