Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation
- Esperón-Moldes, U.
- Ginarte-Val, M.
- Rodríguez-Pazos, L.
- Fachal, L.
- Martín-Santiago, A.
- Vicente, A.
- Jiménez-Gallo, D.
- Guillén-Navarro, E.
- Sampol, L.M.
- González-Enseñat, M.A.
- Vega, A.
Journal:
PLoS ONE
ISSN: 1932-6203
Year of publication: 2020
Volume: 15
Issue: 2
Type: Article