Recessive mutations in SCNM1 are a new cause of Orofaciodigital syndrome due to errors in minor intron splicing affecting primary cilia - Iturrate, A; Rivera-Barahona, A; Flores, CL; Aotaify, G; Elhossini, R; Perez-Sanz, ML; Nevado, J; Tenorio, J; Triviño, JC; Garcia-Gonzalo, FR; Piceci-Sparascio, F; De Luca, A; et al. (European Journal Of Human Genetics, 2024)