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CYP4F22 gene

Known as: CYTOCHROME P450, FAMILY 4, SUBFAMILY F, POLYPEPTIDE 22, FLJ39501, cytochrome P450 family 4 subfamily F member 22 
National Institutes of Health

Papers overview

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2020
2020
Mutations in CYP4F22 cause autosomal recessive congenital ichthyosis (ARCI). However, less than 10% of all ARCI patients carry a… 
Review
2018
Review
2018
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of rare disorders of keratinization characterized by… 
2017
2017
Autosomal recessive congenital ichthyosis (ARCI) caused by mutations in CYP4F22 is very rare. CyP4F22, a protein of the… 
2017
2017
Autosomal recessive congenital ichthyosis (ARCI) is a clinically and genetically heterogeneous group of keratinization disorders… 
Highly Cited
2015
Highly Cited
2015
Significance The sphingolipid backbone ceramide is the major lipid species in the stratum corneum and plays a pivotal function in… 
2011
2011
Background  Mutations in six genes have been identified in autosomal recessive congenital ichthyosis (ARCI). To date, few studies… 
2011
2011
Cytochrome P450s are superfamily of heme proteins which generally monooxygenate hydrophobic compounds. The human cytochrome P450… 
2007
2007
Congenital recessive ichthyoses (CRI) form a remarkably heterogeneous group of diseases, resulting from mutations in at least…