NIDDM with a ceruloplasmin gene mutation

被引：4
作者：
Daimon, M
Yamatani, K
Tominaga, M
Manaka, H
Kato, T
Sasaki, H
机构：
来源：
DIABETES CARE | 1997年 / 20卷 / 04期
关键词：
D O I：
10.2337/diacare.20.4.678a
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：678 / 678
页数：1
相关论文
共 5 条
  • [1] A NONSENSE MUTATION OF THE CERULOPLASMIN GENE IN HEREDITARY CERULOPLASMIN DEFICIENCY WITH DIABETES-MELLITUS
    DAIMON, M
    KATO, T
    KAWANAMI, T
    TOMINAGA, M
    IGARASHI, M
    YAMATANI, K
    SASAKI, H
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 217 (01) : 89 - 95
  • [2] PATHOGENESIS OF NIDDM - A BALANCED OVERVIEW
    DEFRONZO, RA
    BONADONNA, RC
    FERRANNINI, E
    [J]. DIABETES CARE, 1992, 15 (03) : 318 - 368
  • [3] KAHN CR, 1995, NATURE, V373, P384
  • [4] HEREDITARY CERULOPLASMIN DEFICIENCY WITH HEMOSIDEROSIS - A CLINICOPATHOLOGICAL STUDY OF A JAPANESE FAMILY
    MORITA, H
    IKEDA, S
    YAMAMOTO, K
    MORITA, S
    YOSHIDA, K
    NOMOTO, S
    KATO, M
    YANAGISAWA, N
    [J]. ANNALS OF NEUROLOGY, 1995, 37 (05) : 646 - 656
  • [5] A MUTATION IN THE CERULOPLASMIN GENE IS ASSOCIATED WITH SYSTEMIC HEMOSIDEROSIS IN HUMANS
    YOSHIDA, K
    FURIHATA, K
    TAKEDA, S
    NAKAMURA, A
    YAMAMOTO, K
    MORITA, H
    HIYAMUTA, S
    IKEDA, S
    SHIMIZU, N
    YANAGISAWA, N
    [J]. NATURE GENETICS, 1995, 9 (03) : 267 - 272
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