Similar articles for PMID: 10521293

Year	Number of Results
1996	3
1998	2
1999	1
2000	4
2001	6
2002	3
2003	10
2004	4
2005	6
2006	5
2007	4
2008	5
2009	4
2010	4
2011	9
2012	8
2013	9
2014	7
2015	5
2016	9
2017	8
2018	8
2019	15
2020	19
2021	24
2022	18
2023	9
2024	0

1

Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1.

Hardy C, Khanim F, Torres R, Scott-Brown M, Seller A, Poulton J, Collier D, Kirk J, Polymeropoulos M, Latif F, Barrett T. Hardy C, et al. Am J Hum Genet. 1999 Nov;65(5):1279-90. doi: 10.1086/302609. Am J Hum Genet. 1999. PMID: 10521293 Free PMC article.

2

Molecular characterization of WFS1 in patients with Wolfram syndrome.

van ven Ouweland JM, Cryns K, Pennings RJ, Walraven I, Janssen GM, Maassen JA, Veldhuijzen BF, Arntzenius AB, Lindhout D, Cremers CW, Van Camp G, Dikkeschei LD. van ven Ouweland JM, et al. J Mol Diagn. 2003 May;5(2):88-95. doi: 10.1016/s1525-1578(10)60457-6. J Mol Diagn. 2003. PMID: 12707373 Free PMC article.

3

Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.

Gómez-Zaera M, Strom TM, Rodríguez B, Estivill X, Meitinger T, Nunes V. Gómez-Zaera M, et al. Mol Genet Metab. 2001 Jan;72(1):72-81. doi: 10.1006/mgme.2000.3107. Mol Genet Metab. 2001. PMID: 11161832

4

Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.

Giuliano F, Bannwarth S, Monnot S, Cano A, Chabrol B, Vialettes B, Delobel B, Paquis-Flucklinger V; French Group of WS. Giuliano F, et al. Hum Mutat. 2005 Jan;25(1):99-100. doi: 10.1002/humu.9300. Hum Mutat. 2005. PMID: 15605410

5

Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Gene. 2013 Oct 10;528(2):309-13. doi: 10.1016/j.gene.2013.06.040. Epub 2013 Jul 8. Gene. 2013. PMID: 23845777

6

Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.

Gasparin MR, Crispim F, Paula SL, Freire MB, Dalbosco IS, Manna TD, Salles JE, Gasparin F, Guedes A, Marcantonio JM, Gambini M, Salim CP, Moisés RS. Gasparin MR, et al. Eur J Endocrinol. 2009 Feb;160(2):309-16. doi: 10.1530/EJE-08-0698. Epub 2008 Nov 28. Eur J Endocrinol. 2009. PMID: 19042979

7

Identification of a missense variant in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk for type 2 diabetes in Ashkenazi Jewish individuals.

Bansal V, Boehm BO, Darvasi A. Bansal V, et al. Diabetologia. 2018 Oct;61(10):2180-2188. doi: 10.1007/s00125-018-4690-3. Epub 2018 Jul 16. Diabetologia. 2018. PMID: 30014265

8

Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome families.

Domènech E, Gómez-Zaera M, Nunes V. Domènech E, et al. Clin Genet. 2004 Jun;65(6):463-9. doi: 10.1111/j.1399-0004.2004.00249.x. Clin Genet. 2004. PMID: 15151504

9

A single base-pair deletion in the WFS1 gene causes Wolfram syndrome.

Pitt K, James C, Kochar IS, Kapoor A, Jain S, Hussain K, Bennett K. Pitt K, et al. J Pediatr Endocrinol Metab. 2011;24(5-6):389-91. doi: 10.1515/jpem.2011.215. J Pediatr Endocrinol Metab. 2011. PMID: 21823543

10

Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations.

Zenteno JC, Ruiz G, Pérez-Cano HJ, Camargo M. Zenteno JC, et al. Mol Vis. 2008 Jul 25;14:1353-7. Mol Vis. 2008. PMID: 18660851 Free PMC article.

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