• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6-phosphatase gene.

作者信息

Hüner G, Podskarbi T, Schütz M, Baykal T, Sarbat G, Shin Y S, Demirkol M

机构信息

Department of Pediatrics, Istanbul Faculty of Medicine, University of Istanbul, Turkey.

出版信息

J Inherit Metab Dis. 1998 Jun;21(4):445-6. doi: 10.1023/a:1005339616074.

DOI:10.1023/a:1005339616074
PMID:9700612
Abstract
摘要

相似文献

1
Molecular aspects of glycogen storage disease type Ia in Turkish patients: a novel mutation in the glucose-6-phosphatase gene.土耳其糖原贮积病 Ia 型患者的分子特征:葡萄糖-6-磷酸酶基因中的一种新突变
J Inherit Metab Dis. 1998 Jun;21(4):445-6. doi: 10.1023/a:1005339616074.
2
Glucose-6-phosphatase gene mutations in Turkish patients with glycogen storage disease type Ia.土耳其Ia型糖原贮积病患者的葡萄糖-6-磷酸酶基因突变
J Inherit Metab Dis. 2001 Dec;24(8):881-2. doi: 10.1023/a:1013956611607.
3
A common 2 bp deletion mutation in the glucose-6-phosphatase gene in Indian patients with glycogen storage disease type Ia.印度糖原贮积病Ia型患者中葡萄糖-6-磷酸酶基因常见的2个碱基对缺失突变。
J Inherit Metab Dis. 2001 Aug;24(4):517-8. doi: 10.1023/a:1010598109582.
4
Identification of three novel mutations (Q54P, W70X and T108I) in the glucose-6-phosphatase gene of patients with glycogen storage disease type Ia. Mutation in brief no. 256. Online.糖原贮积病 Ia 型患者葡萄糖-6-磷酸酶基因中三个新突变(Q54P、W70X 和 T108I)的鉴定。简讯编号 256。在线版。
Hum Mutat. 1999;14(1):91. doi: 10.1002/(SICI)1098-1004(1999)14:1<91::AID-HUMU21>3.0.CO;2-B.
5
The inheritance of a novel mutation in glycogen storage disease type 1a.1a型糖原贮积病中一种新突变的遗传方式
Biochem Soc Trans. 1996 May;24(2):232S. doi: 10.1042/bst024232s.
6
A novel mutation in the glucose-6-phosphatase gene in Korean twins with glycogen storage disease type Ia.患有Ia型糖原贮积病的韩国双胞胎中葡萄糖-6-磷酸酶基因的一种新突变。
J Inherit Metab Dis. 2000 Dec;23(8):851-2. doi: 10.1023/a:1026777106212.
7
Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia.葡萄糖-6-磷酸酶基因G327A突变在中国I型糖原贮积病患者中很常见。
Hum Mol Genet. 1995 Jun;4(6):1095-6. doi: 10.1093/hmg/4.6.1095.
8
Identification of a novel nonsense mutation (Q24X) in the glucose-6-phosphatase gene of a Portuguese patient with GSD Ia (von Gierke disease).在一名患有糖原贮积病Ia型(冯·吉尔克病)的葡萄牙患者的葡萄糖-6-磷酸酶基因中鉴定出一种新型无义突变(Q24X)。
Hum Mutat. 2000 Nov;16(5):449. doi: 10.1002/1098-1004(200011)16:5<449::AID-HUMU25>3.0.CO;2-L.
9
Glycogen storage disease type 1a in three siblings with the G270V mutation.三名携带G270V突变的兄弟姐妹患1a型糖原贮积病。
J Inherit Metab Dis. 1999 Apr;22(2):149-54. doi: 10.1023/a:1005445802822.
10
Identification of mutations in the glucose-6-phosphatase gene in Czech and Slovak patients with glycogen storage disease type ia, including novel mutations K76N, V166A and 540del5.捷克和斯洛伐克糖原贮积病Ia型患者葡萄糖-6-磷酸酶基因突变的鉴定,包括新突变K76N、V166A和540del5。
Hum Mutat. 2000 Jul;16(1):89. doi: 10.1002/1098-1004(200007)16:1<89::AID-HUMU17>3.0.CO;2-A.

引用本文的文献

1
The induced-fit and catalytic mechanisms of human G6PC1.人葡萄糖-6-磷酸酶催化亚基1的诱导契合和催化机制
Cell Discov. 2025 Jul 15;11(1):62. doi: 10.1038/s41421-025-00814-z.
2
Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease.导致Ia型糖原贮积病的葡萄糖-6-磷酸酶-α(G6PC)基因突变。
Hum Mutat. 2008 Jul;29(7):921-30. doi: 10.1002/humu.20772.
3
Glycogen storage diseases: new perspectives.糖原贮积病:新观点
World J Gastroenterol. 2007 May 14;13(18):2541-53. doi: 10.3748/wjg.v13.i18.2541.
4
Mutation spectrum of type I glycogen storage disease in Hungary.匈牙利I型糖原贮积病的突变谱
J Inherit Metab Dis. 2005;28(6):939-44. doi: 10.1007/s10545-005-0186-7.
5
Glucose-6-phosphatase gene mutations in Turkish patients with glycogen storage disease type Ia.土耳其Ia型糖原贮积病患者的葡萄糖-6-磷酸酶基因突变
J Inherit Metab Dis. 2001 Dec;24(8):881-2. doi: 10.1023/a:1013956611607.
6
Glycogen storage disease type Ia: frequency and clinical course in Turkish children.Ia型糖原贮积病:土耳其儿童的发病率及临床病程
Indian J Pediatr. 2000 Jul;67(7):497-501. doi: 10.1007/BF02760476.