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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 1 |
2010 | 1 |
2017 | 1 |
2024 | 0 |
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Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
Nat Genet. 2006 Nov;38(11):1242-4. doi: 10.1038/ng1893. Epub 2006 Oct 1.
Nat Genet. 2006.
PMID: 17013395
Free PMC article.
Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmus.
Fingert JH, Roos B, Eyestone ME, Pham JD, Mellot ML, Stone E.
Fingert JH, et al.
Ophthalmic Genet. 2010 Jun;31(2):77-80. doi: 10.3109/13816810903584989.
Ophthalmic Genet. 2010.
PMID: 20450309
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Development and clinical utility of a novel diagnostic nystagmus gene panel using targeted next-generation sequencing.
Thomas MG, Maconachie G, Sheth V, McLean RJ, Gottlob I.
Thomas MG, et al.
Eur J Hum Genet. 2017 Jun;25(6):725-734. doi: 10.1038/ejhg.2017.44. Epub 2017 Apr 5.
Eur J Hum Genet. 2017.
PMID: 28378818
Free PMC article.
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