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Literature summary for 4.98.1.1 extracted from

  • Schimmel, R.J.; Van Tuyll Van Serooskerke, A.M.; Bladergroen, R.S.; Van Steensel, A.M.; van Geel, M.; Pasmans, S.G.; Frank, J.
    Exclusion of ferrochelatase gene mutations in patients with seasonal palmoplantar keratoderma (2009), Cell. Mol. Biol. (Noisy-le-grand), 55, 111-117.
    View publication on PubMed

Application

Application Comment Organism
diagnostics mutations in the ferrochelatase gene are not responsible for palmoplantar skin phenotype observed in erythrokeratolysis hiemalis et estivalis of three unrelated Dutch Caucasian patients Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Synonyms

Synonyms Comment Organism
FeCH
-
Homo sapiens
ferrochelatase
-
Homo sapiens

General Information

General Information Comment Organism
malfunction mutations in the ferrochelatase gene are not responsible for palmoplantar skin phenotype observed in erythrokeratolysis hiemalis et estivalis of three unrelated Dutch Caucasian patients Homo sapiens