A. Iturrate Et Al. , "Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia," American Journal of Human Genetics , vol.109, no.10, pp.1828-1849, 2022
Iturrate, A. Et Al. 2022. Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. American Journal of Human Genetics , vol.109, no.10 , 1828-1849.
Iturrate, A., Rivera-Barahona, A., Flores, C., Otaify, G. A., Elhossini, R., Perez-Sanz, M. L., ... Nevado, J.(2022). Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. American Journal of Human Genetics , vol.109, no.10, 1828-1849.
Iturrate, Asier Et Al. "Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia," American Journal of Human Genetics , vol.109, no.10, 1828-1849, 2022
Iturrate, Asier Et Al. "Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia." American Journal of Human Genetics , vol.109, no.10, pp.1828-1849, 2022
Iturrate, A. Et Al. (2022) . "Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia." American Journal of Human Genetics , vol.109, no.10, pp.1828-1849.
@article{article, author={Asier Iturrate Et Al. }, title={Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia}, journal={American Journal of Human Genetics}, year=2022, pages={1828-1849} }