Similar articles for PMID: 14609846

Year	Number of Results
1984	1
1993	1
1995	1
1998	2
2000	5
2001	3
2002	4
2003	4
2004	4
2005	7
2006	3
2007	2
2008	3
2009	3
2010	1
2011	2
2012	5
2013	9
2014	4
2015	8
2016	7
2017	2
2018	7
2019	8
2020	4
2021	8
2022	4
2024	2

1

Genotype-phenotype correlation in British families with X linked congenital stationary night blindness.

Allen LE, Zito I, Bradshaw K, Patel RJ, Bird AC, Fitzke F, Yates JR, Trump D, Hardcastle AJ, Moore AT. Allen LE, et al. Br J Ophthalmol. 2003 Nov;87(11):1413-20. doi: 10.1136/bjo.87.11.1413. Br J Ophthalmol. 2003. PMID: 14609846 Free PMC article.

2

Mutations in the CACNA1F and NYX genes in British CSNBX families.

Zito I, Allen LE, Patel RJ, Meindl A, Bradshaw K, Yates JR, Bird AC, Erskine L, Cheetham ME, Webster AR, Poopalasundaram S, Moore AT, Trump D, Hardcastle AJ. Zito I, et al. Hum Mutat. 2003 Feb;21(2):169. doi: 10.1002/humu.9106. Hum Mutat. 2003. PMID: 12552565

3

A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.

Vincent A, Wright T, Day MA, Westall CA, Héon E. Vincent A, et al. Mol Vis. 2011;17:3262-70. Epub 2011 Dec 15. Mol Vis. 2011. PMID: 22194652 Free PMC article.

4

Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.

Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, Riemslag FC, van Schooneveld MJ, Kappers AM, van Genderen MM. Bijveld MM, et al. Ophthalmology. 2013 Oct;120(10):2072-81. doi: 10.1016/j.ophtha.2013.03.002. Epub 2013 May 25. Ophthalmology. 2013. PMID: 23714322

5

Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.

Nakamura M, Ito S, Terasaki H, Miyake Y. Nakamura M, et al. Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1610-6. Invest Ophthalmol Vis Sci. 2001. PMID: 11381068

6

Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.

Pasutto F, Ekici A, Reis A, Kremers J, Huchzermeyer C. Pasutto F, et al. Ophthalmic Genet. 2018 Dec;39(6):741-748. doi: 10.1080/13816810.2018.1520263. Epub 2018 Sep 27. Ophthalmic Genet. 2018. PMID: 30260717

7

A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.

Kondo M, Das G, Imai R, Santana E, Nakashita T, Imawaka M, Ueda K, Ohtsuka H, Sakai K, Aihara T, Kato K, Sugimoto M, Ueno S, Nishizawa Y, Aguirre GD, Miyadera K. Kondo M, et al. PLoS One. 2015 Sep 14;10(9):e0137072. doi: 10.1371/journal.pone.0137072. eCollection 2015. PLoS One. 2015. PMID: 26368928 Free PMC article.

8

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

Zeitz C, Minotti R, Feil S, Mátyás G, Cremers FP, Hoyng CB, Berger W. Zeitz C, et al. Mol Vis. 2005 Mar 2;11:179-83. Mol Vis. 2005. PMID: 15761389 Free article.

9

Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.

McAnany JJ, Alexander KR, Kumar NM, Ying H, Anastasakis A, Fishman GA. McAnany JJ, et al. Ophthalmic Genet. 2013 Sep;34(3):167-73. doi: 10.3109/13816810.2012.743570. Epub 2013 Jan 4. Ophthalmic Genet. 2013. PMID: 23289809 Free PMC article.

10

Behavioral phenotypic properties of a natural occurring rat model of congenital stationary night blindness with Cacna1f mutation.

An J, Wang L, Guo Q, Li L, Xia F, Zhang Z. An J, et al. J Neurogenet. 2012 Sep;26(3-4):363-73. doi: 10.3109/01677063.2012.684416. Epub 2012 Jul 16. J Neurogenet. 2012. PMID: 22800190

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