Letter to Editor
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Herediter hemokromatozun nadir bir nedeni: homozigot H63D

Year 2018, Volume: 43 Number: Supplement 1, 330 - 332, 29.12.2018

Cengiz Beyan Esin Beyan

https://doi.org/10.17826/cumj.418297

Abstract

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Keywords

demir aşırı yükü hemokromatozis İnsan HFE proteini

References

  • 1

A rare cause of hereditary hemochromatosis: homozygous H63D

Year 2018, Volume: 43 Number: Supplement 1, 330 - 332, 29.12.2018

Cengiz Beyan Esin Beyan

https://doi.org/10.17826/cumj.418297

Abstract

-

Keywords

hereditary hemochromatosis

References

  • 1
There are 1 citations in total.

Details

Primary Language Turkish
Subjects Health Care Administration
Journal Section Letter to the Editor
Authors

Cengiz Beyan 0000-0003-1716-539X

Esin Beyan 0000-0001-7263-2099

Publication Date December 29, 2018
Acceptance Date May 12, 2018
Published in Issue Year 2018 Volume: 43 Number: Supplement 1

Cite

MLA Beyan, Cengiz and Esin Beyan. “Herediter Hemokromatozun Nadir Bir Nedeni: Homozigot H63D”. Cukurova Medical Journal, vol. 43, no. Ek 1, 2018, pp. 330-2, doi:10.17826/cumj.418297.
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