Combination of heterozygous APOB gene mutation with PNPLA3 and TM6SF2 variants promotes steatotic liver disease, cirrhosis and HCC development
Résumé
No abstract available
Mots clés
Humans
Male
Female
Middle Aged
Apolipoprotein B-100/genetics
Nash
*Mutation
*Lipase/genetics
familial hypobetalipoproteinemia
Nafld
Apolipoprotein B
Fhbl
Masld
Snp
*Carcinoma
Hepatocellular/genetics
*Heterozygote
*Liver Cirrhosis/genetics
*Liver Neoplasms/genetics
*Membrane Proteins/genetics
Acyltransferases
Fatty Liver/genetics
Fhbl-sd2
Phospholipases A2
Calcium-Independent
Domaines
Sciences du Vivant [q-bio]Origine | Publication financée par une institution |
---|---|
Licence |