Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.

Haematologica

Volumn 91, Issue 8 Suppl, 2006, Pages

  Majore, S ^a   Milano, F ^a   Binni, F ^a   Stuppia, L ^a   Cerrone, A ^a   Tafuri, A ^a   De Bernardo, C ^a   Palka, G ^a   Grammatico, P ^a  

^a SAN CAMILLO FORLANINI HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

TFR2 PROTEIN, HUMAN; TRANSFERRIN; TRANSFERRIN RECEPTOR;

ADULT; ARTICLE; FAMILY; FEMALE; GENETIC PREDISPOSITION; GENETICS; HEMOCHROMATOSIS; HUMAN; IRON OVERLOAD; ITALY; MALE; METABOLISM; NUCLEOTIDE SEQUENCE;

ADULT; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEMOCHROMATOSIS; HUMANS; IRON OVERLOAD; ITALY; MALE; RECEPTORS, TRANSFERRIN; TRANSFERRIN;

EID: 33749075204     PISSN: None     EISSN: 15928721     Source Type: Journal    
DOI: None     Document Type: Article

References (0)