A frequent keratin 8 p.L227L polymorphism, but no point mutations in keratin 8 and 18 genes, in patients with various liver disorders.

Journal of medical genetics

Volumn 41, Issue 4, 2004, Pages

  Hesse, M ^a   Berg, T ^a   Wiedenmann, B ^a   Spengler, U ^a   Woitas, R P ^a   Magin, T M ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKERATIN 8; KERATIN; KRT8 PROTEIN, HUMAN;

GENE FREQUENCY; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; HUMAN; LETTER; LIVER DISEASE; NUCLEOTIDE SEQUENCE; POINT MUTATION;

DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; KERATIN-8; KERATINS; LIVER DISEASES; POINT MUTATION; POLYMORPHISM, GENETIC;

EID: 2342524657     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2003.012393     Document Type: Letter

References (0)