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.