Herediter hemokromatozun nadir bir nedeni: homozigot H63D
-
Main Authors: | Cengiz BEYAN, Esin BEYAN |
---|---|
Format: | Article |
Language: | English |
Published: |
Cukurova University
2018-12-01
|
Series: | Cukurova Medical Journal |
Subjects: | |
Online Access: | https://dergipark.org.tr/tr/pub/cumj/issue/38921/418297?publisher=cu |
Similar Items
-
Mutations in the HFE gene (C282Y, H63D, S65C) in a Brazilian population Mutações no gene HFE (C282Y, H63D, S65C) em uma população brasileira
by: Simone Bueno, et al.
Published: (2006-12-01) -
Juvenile Hemochromatosis: Rheumatic Manifestations of 2 Sisters Responding to Deferasirox Treatment. A Case Series and Literature Review
by: Alqanatish J, et al.
Published: (2021-01-01) -
Therapeutic Erythrocytapheresis in the Initial Treatment of Hereditary Hemochromatosis
by: Vít Řeháček, et al.
Published: (2012-01-01) -
Possible roles of the hereditary hemochromatosis protein, HFE, in regulating cellular iron homeostasis
by: CAROLINE A ENNS
Published: (2006-01-01) -
Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City
by: Héctor A. Baptista-González;, et al.
Published: (2007-01-01)