Significance of the 'minor' genetic mutations in hereditary hemochromatosis. Report of two cases;Significato delle mutazioni genetiche 'minori' nell'ambito dell'emocromatosi ereditaria: A proposito di due casi clinici

Annali Italiani di Medicina Interna

Volumn 15, Issue 3, 2000, Pages 221-225

  Maccari, S ^a   Plancher, A C ^a  

^a Arcispedale S Maria Nuova   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; GENE MUTATION; HEMOCHROMATOSIS; HEPATITIS C VIRUS; HUMAN; IRON OVERLOAD; LIVER BIOPSY; MALE; BIOPSY; BLOOD; COMPARATIVE STUDY; GENETICS; HEPATITIS C; HETEROZYGOTE; HOMOZYGOTE; LIVER; MUTATION; PATHOLOGY; PHENOTYPE; PHLEBOTOMY;

FERRITIN;

ADULT; BIOPSY; FERRITINS; HEMOCHROMATOSIS; HEPATITIS C, CHRONIC; HETEROZYGOTE; HOMOZYGOTE; HUMANS; LIVER; MALE; MUTATION; PHENOTYPE; PHLEBOTOMY;

EID: 0033623524     PISSN: 03939340     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

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