Heredity of idiopathic haemochromatosis.
作者信息
Simon M, Bourel M, Genetet B, Fauchet R
出版信息
Lancet. 1977 Mar 26;1(8013):706. doi: 10.1016/s0140-6736(77)92152-3.
PMID:66508
Abstract
摘要
相似文献
1
Heredity of idiopathic haemochromatosis.特发性血色素沉着症的遗传
Lancet. 1977 Mar 26;1(8013):706. doi: 10.1016/s0140-6736(77)92152-3.
2
[Heredity in idiopathic hemochromatosis: evidence of recessive transmission and of the location of the responsible gene on chromosome 6].[特发性血色素沉着症的遗传：隐性遗传证据及致病基因在6号染色体上的定位]
Gastroenterol Clin Biol. 1978;2(6-7):573-7.
3
Inheritance of idiopathic haemochromatosis.特发性血色素沉着症的遗传
Lancet. 1977 May 21;1(8021):1106-7.
4
HLA determinants in idiopathic haemochromatosis.特发性血色素沉着症中的人类白细胞抗原决定簇
Dan Med Bull. 1985 Oct;32(5):262-4.
5
[Idiopathic hemochromatosis: association with antigens of the HLA system].
Med Klin (Munich). 1991 Oct 15;86(10):503-7.
6
Genetic mapping of the hemochromatosis locus on chromosome six.6号染色体上血色素沉着病基因座的基因定位
Hum Immunol. 1980 Jul;1(1):19-22. doi: 10.1016/0198-8859(80)90005-1.
7
Idiopathic haemochromatosis: an autosomal recessive disease.特发性血色素沉着症：一种常染色体隐性疾病。
Clin Genet. 1974;5(3):234-41. doi: 10.1111/j.1399-0004.1974.tb01688.x.
8
9
Histocompatibility antigens as markers of abnormal iron metabolism in patients with idiopathic haemochromatosis and their relatives.
Lancet. 1977 Feb 12;1(8007):327-9. doi: 10.1016/s0140-6736(77)91133-3.
10
[Idiopathic haemochromatosis. Pathogenic and genetic aspects. Detection and prevention (author's transl)].[特发性血色素沉着症。发病机制与遗传学方面。检测与预防（作者译）]
Nouv Presse Med. 1979 Mar 17;8(13):1083-7.
引用本文的文献
1
HFE-Related Hemochromatosis May Be a Primary Kupffer Cell Disease.与HFE相关的血色素沉着症可能是一种原发性库普弗细胞疾病。
Biomedicines. 2025 Mar 10;13(3):683. doi: 10.3390/biomedicines13030683.
2
Inherited Disorders of Iron Overload.遗传性铁过载疾病
Front Nutr. 2018 Oct 29;5:103. doi: 10.3389/fnut.2018.00103. eCollection 2018.
Zotero 插件