Condition: Cirrhosis, Familial


rs57370769 in KRT18 gene and Cirrhosis, Familial PMID 12724528 2003 Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.

PMID 9011570 1997 Mutation of human keratin 18 in association with cryptogenic cirrhosis.

rs57354642 in KRT18;KRT8 gene and Cirrhosis, Familial PMID 12724528 2003 Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.

PMID 9011570 1997 Mutation of human keratin 18 in association with cryptogenic cirrhosis.

rs61710484 in KRT8 gene and Cirrhosis, Familial PMID 12724528 2003 Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.

rs57758506 in KRT8;KRT18 gene and Cirrhosis, Familial PMID 9011570 1997 Mutation of human keratin 18 in association with cryptogenic cirrhosis.

PMID 12724528 2003 Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.