Concepedia

Publication | Open Access

Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia

DOIFull Paper Access

14

Citations

54

References

2022

Year

Asier Iturrate, Ana Rivera‐Barahona, Carmen‐Lisset Flores, Ghada A. Otaify, Rasha M. Elhossini, Marina Leonor Pérez-Sanz, Julián Nevado, Jair Tenorio, Juan Carlos Triviño, Francesc R. García-Gonzalo,
The American Journal of Human Genetics

References

YearCitations

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