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Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation

2020- Esperón Moldes, Uxía Saraiva; Ginarte Val, Manuel Javier; Rodríguez Pazos, Laura; Fachal Vilar, Laura; Martín-Santiago, A.; [et al.]