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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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2019
2019
Ictioses Congénitas: Série de 11 Casos da Consulta Multidisciplinar de Dermatologia Pediátrica, Centro Hospitalar e Universitário de Lisboa Central
Introdução: As ictioses são um grupo heterogéneo de distúrbios genéticos hereditários que ocorrem devido a um defeito da… 
2019
2019
Congenital Ichthyoses: 11 Cases from the Pediatric Dermatology Multidisciplinary Consultation of the Centro Hospitalar e Universitário de Lisboa Central
Introduction : Congenital ichthyoses are a heterogeneous group of hereditary genetic disorders that occur due to a defective… 
2017
2017
Two missense mutations in CYP4F22 in autosomal recessive congenital ichthyosis
Autosomal recessive congenital ichthyosis (ARCI) is a clinically and genetically heterogeneous group of keratinization disorders… 
2017
2017
A case of lamellar ichthyosis due to a novel TGM1 mutation associated with Parkinson’s disease
The transglutaminase 1 (TGM1) gene is a major causative gene of autosomal recessive congenital ichthyoses (ARCI), including… 
Review
2017
Review
2017
EVIEW utosomal Recessive Congenital Ichthyosis
The term autosomal recessive congenital ichthyosis (ARCI) refers to a group of rare disorders of keratinization classified as… 
2011
2011
Molecular modeling and identification of substrate binding site of orphan human cytochrome P450 4F22
Cytochrome P450s are superfamily of heme proteins which generally monooxygenate hydrophobic compounds. The human cytochrome P450… 
2008
2008
Rapid detection of homozygous mutations in congenital recessive ichthyosis
Congenital recessive ichthyoses (CRI) form a remarkably heterogeneous group of diseases, resulting from mutations in at least… 
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