Extremely rare association of HFE mutations with porphyria cutanea tarda in Japanese patients

被引：19

作者：

Furuyama, K ^{[1
]}

Kondo, M

Hirata, K

Fujita, H

Sassa, S

机构：

[1] Tohoku Univ, Sch Med, Dept Biochem, Sendai, Miyagi 980, Japan

[2] Rockefeller Univ, New York, NY 10021 USA

[3] Inst Publ Hlth, Tokyo 108, Japan

[4] Hokkaido Univ, Sch Med, Sapporo, Hokkaido 060, Japan

来源：

HEPATOLOGY | 1999年 / 30卷 / 06期

关键词：

D O I：

10.1002/hep.510300627

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：1532 / 1533

页数：2

共 7 条

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

Feder, JN ;

Gnirke, A ;

Thomas, W ;

Tsuchihashi, Z ;

Ruddy, DA ;

Basava, A ;

Dormishian, F ;

Domingo, R ;

Ellis, MC ;

Fullan, A ;

Hinton, LM ;

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 ;

Quintana, L ;

Starnes, SM ;

Schatzman, RC ;

Brunke, KJ ;

Drayna, DT ;

Risch, NJ ;

Bacon, BR ;

Wolff, RK .

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

[2]

Kappas A., 1995, METABOLIC MOL BASES, P2103

[3] Global prevalence of putative haemochromatosis mutations [J].

MerryweatherClarke, AT ;

Pointon, JJ ;

Shearman, JD ;

Robson, KJH .

JOURNAL OF MEDICAL GENETICS, 1997, 34 (04) :275-278

[4] Screening of patients with iron overload to identify hemochromatosis and porphyria cutanea tarda [J].

OReilly, FM ;

Darby, C ;

Fogarty, J ;

Tormey, W ;

Kay, EW ;

Leader, M ;

Murphy, GM .

ARCHIVES OF DERMATOLOGY, 1997, 133 (09) :1098-1101

[5] The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda [J].

Roberts, AG ;

Whatley, SD ;

Nicklin, S ;

Worwood, M ;

Pointon, JJ ;

Stone, C ;

Elder, GH .

HEPATOLOGY, 1997, 25 (01) :159-161

[6]

Sampietro M, 1999, HAEMATOLOGICA, V84, P248

[7] Frequencies in the Japanese population of HFE gene mutations [J].

Sohda, T ;

Yanai, J ;

Soejima, H ;

Tamura, K .

BIOCHEMICAL GENETICS, 1999, 37 (1-2) :63-68

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