Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload. | Haematologica;91(8 Suppl): ECR33, 2006 Aug. | MEDLINE

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

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

Affiliation

Majore S; Medical Genetics, University La Sapienza S. Camillo-Forlanini Hospital, Rome, Italy.

Haematologica ; 91(8 Suppl): ECR33, 2006 Aug.

Article in En | MEDLINE | ID: mdl-16923517

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Transferrin / Iron Overload / Genetic Predisposition to Disease / Hemochromatosis Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Haematologica Year: 2006 Document type: Article Affiliation country: Country of publication:

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Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Transferrin / Iron Overload / Genetic Predisposition to Disease / Hemochromatosis Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Haematologica Year: 2006 Document type: Article Affiliation country: Country of publication: