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3. Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency. Minucci A; Concolino P; Antenucci M; Santonocito C; Ameglio F; Zuppi C; Giardina B; Capoluongo E Clin Biochem; 2007 Aug; 40(12):856-8. PubMed ID: 17524386 [TBL] [Abstract][Full Text] [Related]
4. Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations. Yan T; Cai R; Mo O; Zhu D; Ouyang H; Huang L; Zhao M; Huang F; Li L; Liang X; Xu X Haematologica; 2006 Oct; 91(10):1321-8. PubMed ID: 17018380 [TBL] [Abstract][Full Text] [Related]
5. [The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province]. Yang Z; Chu J; Xu S; Lin K; Tao Y; Shi L Zhonghua Xue Ye Xue Za Zhi; 2000 Oct; 21(10):509-11. PubMed ID: 11877026 [TBL] [Abstract][Full Text] [Related]
6. [Glucose-6-phosphate dehydrogenase mutations among Cantonese revealed by polymerase chain reaction using dried blood spots]. Tang D; Ma X; Song C Zhonghua Xue Ye Xue Za Zhi; 1998 Apr; 19(4):189-91. PubMed ID: 11243133 [TBL] [Abstract][Full Text] [Related]
7. A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. Online. Galanello R; Loi D; Sollaino C; Dessì S; Cao A; Melis MA Hum Mutat; 1998; 12(1):72-3. PubMed ID: 10627140 [TBL] [Abstract][Full Text] [Related]
8. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Jordan. Karadsheh NS; Moses L; Ismail SI; Devaney JM; Hoffman E Haematologica; 2005 Dec; 90(12):1693-4. PubMed ID: 16330444 [TBL] [Abstract][Full Text] [Related]
9. Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene. Vulliamy T; Beutler E; Luzzatto L Hum Mutat; 1993; 2(3):159-67. PubMed ID: 8364584 [TBL] [Abstract][Full Text] [Related]
11. [Studies on glucose-6-phosphate dehydrogenase (G6PD) deficiency in China: forty years retrospection and perspective]. Du C Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):174-5. PubMed ID: 12894787 [No Abstract] [Full Text] [Related]
12. G6PDdb, an integrated database of glucose-6-phosphate dehydrogenase (G6PD) mutations. Kwok CJ; Martin AC; Au SW; Lam VM Hum Mutat; 2002 Mar; 19(3):217-24. PubMed ID: 11857737 [TBL] [Abstract][Full Text] [Related]
13. The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of Senegal. De Araujo C; Migot-Nabias F; Guitard J; Pelleau S; Vulliamy T; Ducrocq R Haematologica; 2006 Feb; 91(2):262-3. PubMed ID: 16461316 [TBL] [Abstract][Full Text] [Related]
14. Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency. Minucci A; Concolino P; Vendittelli F; Giardina B; Zuppi C; Capoluongo E Clin Biochem; 2008 Jun; 41(9):742-5. PubMed ID: 18086567 [TBL] [Abstract][Full Text] [Related]
16. A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case Report. Jang MA; Kim JY; Lee KO; Kim SH; Koo HH; Kim HJ Ann Clin Lab Sci; 2015; 45(4):446-8. PubMed ID: 26275698 [TBL] [Abstract][Full Text] [Related]
17. Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews. Karimi M; Yavarian M; Afrasiabi A; Dehbozorgian J; Rachmilewitz E Arch Med Res; 2008 Feb; 39(2):212-4. PubMed ID: 18164966 [TBL] [Abstract][Full Text] [Related]
18. G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population. Minucci A; Antenucci M; Giardina B; Zuppi C; Capoluongo E Clin Biochem; 2010 Sep; 43(13-14):1180-1. PubMed ID: 20621077 [No Abstract] [Full Text] [Related]
19. Rapid and simple identification of the commonest glucose-6-phosphate dehydrogenase (G6PD) Italian mutations: from DNA extraction to genotyping. Minucci A; Gentile L; Zuppi C; Giardina B; Capoluongo E Clin Chim Acta; 2012 Jun; 413(11-12):1018-9. PubMed ID: 22326377 [No Abstract] [Full Text] [Related]
20. Marked decrease in specific activity contributes to disease phenotype in two human glucose 6-phosphate dehydrogenase mutants, G6PD(Union) and G6PD(Andalus). Wang XT; Lam VM; Engel PC Hum Mutat; 2005 Sep; 26(3):284. PubMed ID: 16088936 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]