The clinical penetrance of hereditary hemochromatosis

被引：7

作者：

Beutler, E

Felitti, VJ

机构：

[1] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA

[2] Kaiser Permanente, Dept Prevent Med, San Diego, CA USA

来源：

HEPATOLOGY | 2003年 / 37卷 / 03期

关键词：

D O I：

10.1053/jhep.2003.50080

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

引用

页码：711 / 711

页数：1

共 8 条

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[2]

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[3] Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA [J].

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Ho, NJ ;

Gelbart, T .

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

[4] Clinical haemochromatosis in HFE mutation carriers - Authors' reply [J].

Beutler, E ;

Felitti, V ;

Koziol, JA ;

Gelbart, T .

LANCET, 2002, 360 (9330) :413-414

[5]

Cox T, 2002, LANCET, V360, P412, DOI 10.1016/S0140-6736(02)09582-X

[6] Seeking candidate mutations that affect iron homeostasis [J].

Lee, P ;

Gelbart, T ;

West, C ;

Halloran, C ;

Beutler, E .

BLOOD CELLS MOLECULES AND DISEASES, 2002, 29 (03) :471-487

[7] Clinical haemochromatosis in HFE mutation carriers [J].

Poullis, A ;

Moodie, SJ ;

Maxwell, JD .

LANCET, 2002, 360 (9330) :411-412

[8] Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene [J].

Waalen, J ;

Felitti, V ;

Gelbart, T ;

Ho, NJ ;

Beutler, E .

MAYO CLINIC PROCEEDINGS, 2002, 77 (06) :522-530

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