These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the young. Mantovani V; Salardi S; Cerreta V; Bastia D; Cenci M; Ragni L; Zucchini S; Parente R; Cicognani A Hum Mutat; 2003 Oct; 22(4):338. PubMed ID: 12955723 [TBL] [Abstract][Full Text] [Related]
3. [Mutation screening of GCK gene in Chinese early-onset diabetes population]. Zheng TS; Wu SH; Yang Z; Lu HJ; Xiang KS Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):671-4. PubMed ID: 16331569 [TBL] [Abstract][Full Text] [Related]
5. Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY). Toaima D; Näke A; Wendenburg J; Praedicow K; Rohayem J; Engel K; Galler A; Gahr M; Lee-Kirsch MA Hum Mutat; 2005 May; 25(5):503-4. PubMed ID: 15841481 [TBL] [Abstract][Full Text] [Related]
6. Genetic and clinical characteristics of Korean maturity-onset diabetes of the young (MODY) patients. Hwang JS; Shin CH; Yang SW; Jung SY; Huh N Diabetes Res Clin Pract; 2006 Oct; 74(1):75-81. PubMed ID: 16632067 [TBL] [Abstract][Full Text] [Related]
7. Identification of eight new mutations in the GCK gene by DHPLC screening in a Spanish population. Solera J; Arias P; Amiñoso C; González-Casado I; Garre P; Herranz L; Villarroel A; Cruz M; Jáñez M; Pallardo LF; Gracia R Diabetes Res Clin Pract; 2009 Jul; 85(1):20-3. PubMed ID: 19410318 [TBL] [Abstract][Full Text] [Related]
8. Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing. López-Garrido MP; Herranz-Antolín S; Alija-Merillas MJ; Giralt P; Escribano J Clin Endocrinol (Oxf); 2013 Sep; 79(3):342-7. PubMed ID: 23009393 [TBL] [Abstract][Full Text] [Related]
9. Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain. Estalella I; Rica I; Perez de Nanclares G; Bilbao JR; Vazquez JA; San Pedro JI; Busturia MA; Castaño L; Clin Endocrinol (Oxf); 2007 Oct; 67(4):538-46. PubMed ID: 17573900 [TBL] [Abstract][Full Text] [Related]
10. Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients. Xu JY; Dan QH; Chan V; Wat NM; Tam S; Tiu SC; Lee KF; Siu SC; Tsang MW; Fung LM; Chan KW; Lam KS Eur J Hum Genet; 2005 Apr; 13(4):422-7. PubMed ID: 15657605 [TBL] [Abstract][Full Text] [Related]
11. Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy. Gloyn AL Hum Mutat; 2003 Nov; 22(5):353-62. PubMed ID: 14517946 [TBL] [Abstract][Full Text] [Related]
12. Three novel missense mutations in the glucokinase gene (G80S; E221K; G227C) in Italian subjects with maturity-onset diabetes of the young (MODY). Mutations in brief no. 162. Online. Guazzini B; Gaffi D; Mainieri D; Multari G; Cordera R; Bertolini S; Pozza G; Meschi F; Barbetti F Hum Mutat; 1998; 12(2):136. PubMed ID: 10694920 [TBL] [Abstract][Full Text] [Related]
13. A novel nonsense mutation in GCK exon 9 co-segregates with diabetes phenotype. Knebel B; Jacob S; Boxberg CV; Müller-Wieland D; Kotzka J Exp Clin Endocrinol Diabetes; 2004 Jun; 112(6):298-301. PubMed ID: 15216446 [TBL] [Abstract][Full Text] [Related]
14. GCK and HNF1A mutations in Canadian families with maturity onset diabetes of the young (MODY). Cao H; Shorey S; Robinson J; Metzger DL; Stewart L; Cummings E; Hegele RA Hum Mutat; 2002 Dec; 20(6):478-9. PubMed ID: 12442280 [TBL] [Abstract][Full Text] [Related]
15. Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations. Pruhova S; Dusatkova P; Sumnik Z; Kolouskova S; Pedersen O; Hansen T; Cinek O; Lebl J Pediatr Diabetes; 2010 Dec; 11(8):529-35. PubMed ID: 20337973 [TBL] [Abstract][Full Text] [Related]
16. [Swiss journey through the clinical and genetic characteristics of diabetes in young patients]. Dussoix P; Tappy L; Philippe J Schweiz Med Wochenschr; 1998 Jan; 128(5):162-6. PubMed ID: 9522422 [TBL] [Abstract][Full Text] [Related]
17. Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes. Stoffel M; Patel P; Lo YM; Hattersley AT; Lucassen AM; Page R; Bell JI; Bell GI; Turner RC; Wainscoat JS Nat Genet; 1992 Oct; 2(2):153-6. PubMed ID: 1303265 [TBL] [Abstract][Full Text] [Related]
18. Three novel mutations in MODY and its phenotype in three different Czech families. Bazalová Z; Rypácková B; Broz J; Brunerová L; Polák J; Rusavý Z; Treslová L; Andel M Diabetes Res Clin Pract; 2010 May; 88(2):132-8. PubMed ID: 20132997 [TBL] [Abstract][Full Text] [Related]
19. Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene. Bennett K; James C; Mutair A; Al-Shaikh H; Sinani A; Hussain K Pediatr Diabetes; 2011 May; 12(3 Pt 1):192-6. PubMed ID: 21518409 [TBL] [Abstract][Full Text] [Related]