A genotype-phenotype correlation between null-allele mutations in the ferrochelatase gene and liver complication in patients with erythropoietic protoporphyria.

Cellular and molecular biology (Noisy-le-Grand, France)

Volumn 48, Issue 1, 2002, Pages 91-96

  Minder, E I ^a   Gouya, L ^a   Schneider Yin, X ^a   Deybach, J C ^a  

^a TRIEMLI HOSPITAL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

FERROCHELATASE;

ALLELE; ARTICLE; CONGENITAL ERYTHROPOIETIC PORPHYRIA; ENZYMOLOGY; FRAMESHIFT MUTATION; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; HUMAN; INCIDENCE; LIVER DISEASE; MUTATION; PHENOTYPE; STOP CODON;

ALLELES; CODON, NONSENSE; FERROCHELATASE; FRAMESHIFT MUTATION; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INCIDENCE; LIVER DISEASES; MUTATION; PHENOTYPE; PORPHYRIA, ERYTHROPOIETIC;

EID: 0036483671     PISSN: 01455680     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)