Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene:: case control study of 492 French centenarians

被引：36

作者：

Coppin, H

Bensaid, M

Fruchon, S

Borot, N

Blanché, H

Roth, MP ^{[1
]}

机构：

[1] CHU Purpan, Unite Physiopathol Cellulaire, CNRS, UPR 2163, F-31059 Toulouse 3, France

[2] Fdn Jean Dausset, Ctr Etud Polymorphisme Humain, F-75010 Paris, France

来源：

BRITISH MEDICAL JOURNAL | 2003年 / 327卷 / 7407期

关键词：

D O I：

10.1136/bmj.327.7407.132

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：132 / 133

页数：2

共 5 条

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LANCET, 2002, 359 (9302) :211-218

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[3] Use of denaturing HPLC and a heteroduplex generator to detect the HFE C282Y mutation associated with genetic hemochromatosis [J].

Fruchon, S ;

Bensaid, M ;

Borot, N ;

Roth, MP ;

Coppin, H .

CLINICAL CHEMISTRY, 2003, 49 (05) :822-824

[4] Morbidity risk in HFE associated hereditary hemochromatosis C282Y heterozygotes [J].

Fuchs, J ;

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Kaufmann, R .

TOXICOLOGY, 2002, 180 (02) :169-181

[5] HFE Mutations as risk factors in disease [J].

Worwood, M .

BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2002, 15 (02) :295-314

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