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Year | Number of Results |
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1999 | 1 |
2006 | 2 |
2015 | 1 |
2016 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 57497
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Heterozygous deletion of the LRFN2 gene is associated with working memory deficits.
Eur J Hum Genet. 2016 Jun;24(6):911-8. doi: 10.1038/ejhg.2015.221. Epub 2015 Oct 21.
Eur J Hum Genet. 2016.
PMID: 26486473
Free PMC article.
Comparative analysis of structure, expression and PSD95-binding capacity of Lrfn, a novel family of neuronal transmembrane proteins.
Morimura N, Inoue T, Katayama K, Aruga J.
Morimura N, et al.
Gene. 2006 Oct 1;380(2):72-83. doi: 10.1016/j.gene.2006.05.014. Epub 2006 Jun 3.
Gene. 2006.
PMID: 16828986
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A novel family of adhesion-like molecules that interacts with the NMDA receptor.
Wang CY, Chang K, Petralia RS, Wang YX, Seabold GK, Wenthold RJ.
Wang CY, et al.
J Neurosci. 2006 Feb 22;26(8):2174-83. doi: 10.1523/JNEUROSCI.3799-05.2006.
J Neurosci. 2006.
PMID: 16495444
Free PMC article.
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Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Ishikawa K, Kikuno R, Hirosawa M, Nomura N, Ohara O.
Nagase T, et al.
DNA Res. 1999 Oct 29;6(5):337-45. doi: 10.1093/dnares/6.5.337.
DNA Res. 1999.
PMID: 10574462
Free article.
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