Catalase abnormality in a Caucasian family in the United States.
An erythrocyte catalase with atypical electromigration velocity was discovered in three generations of a family of Scandinavian-British extraction. Six members are heterozygous for the hereditary autosomal character; no abnormal homozygotes were found. The condition is associated with normal erythrocyte catalase activity and with no clinical or subclinical disease.
D002374:Catalase; D004912:Erythrocytes; D006579:Heterozygote; D006720:Homozygote; D006801:Humans; D014481:United States
D002374:Catalase
CATALASE