Commentary

被引：8

作者：

Beutler, E ^{[1
]}

机构：

[1] KAISER PERMANENTE, SAN DIEGO, CA USA

来源：

BLOOD CELLS MOLECULES AND DISEASES | 1997年 / 23卷 / 08期

关键词：

D O I：

10.1006/bcmd.1997.0130

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：A145 / +

页数：2

共 6 条

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BLOOD CELLS MOLECULES AND DISEASES, 1997, 23 (08) :135-145

[2]

Beutler Ernest, 1996, Blood Cells Molecules and Diseases, V22, P187, DOI 10.1006/bcmd.1996.0027

[3] Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients [J].

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Coppin, H .

IMMUNOGENETICS, 1997, 45 (05) :320-324

[4]

Carella M, 1997, AM J HUM GENET, V60, P828

[5] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [J].

Feder, JN ;

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Ellis, MC ;

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Jones, NL ;

Kimmel, BE ;

Kronmal, GS ;

Lauer, P ;

Lee, VK ;

Loeb, DB ;

Mapa, FA ;

McClelland, E ;

Meyer, NC ;

Mintier, GA ;

Moeller, N ;

Moore, T ;

Morikang, E ;

Prass, CE ;

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Wolff, RK .

NATURE GENETICS, 1996, 13 (04) :399-408

[6] Haemochromatosis and HLA-H [J].

Jouanolle, AM ;

Gandon, G ;

Jezequel, P ;

Blayau, M ;

Campion, ML ;

Yaouanq, J ;

Mosser, J ;

Fergelot, P ;

Chauvel, B ;

Bouric, P ;

Carn, G ;

Andrieux, N ;

Gicquel, I ;

LeGall, JY ;

David, V .

NATURE GENETICS, 1996, 14 (03) :251-252

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