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A novel mutation in CLCN1 associated with feline myotonia congenita.
Gandolfi B, Daniel RJ, O'Brien DP, Guo LT, Youngs MD, Leach SB, Jones BR, Shelton GD, Lyons LA. Gandolfi B, et al. Among authors: lyons la. PLoS One. 2014 Oct 30;9(10):e109926. doi: 10.1371/journal.pone.0109926. eCollection 2014. PLoS One. 2014. PMID: 25356766 Free PMC article.
Myopathy with tubulin-reactive inclusions in two cats.
Shelton GD, Sturges BK, Lyons LA, Williams DC, Aleman M, Jiang Y, Mizisin AP. Shelton GD, et al. Among authors: lyons la. Acta Neuropathol. 2007 Nov;114(5):537-42. doi: 10.1007/s00401-007-0217-6. Epub 2007 Mar 29. Acta Neuropathol. 2007. PMID: 17393175
The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71.
Gandolfi B, Outerbridge CA, Beresford LG, Myers JA, Pimentel M, Alhaddad H, Grahn JC, Grahn RA, Lyons LA. Gandolfi B, et al. Among authors: lyons la. Mamm Genome. 2010 Oct;21(9-10):509-15. doi: 10.1007/s00335-010-9290-6. Epub 2010 Oct 16. Mamm Genome. 2010. PMID: 20953787 Free PMC article.
A high-resolution 15,000(Rad) radiation hybrid panel for the domestic cat.
Bach LH, Gandolfi B, Grahn JC, Millon LV, Kent MS, Narfstrom K, Cole SA, Mullikin JC, Grahn RA, Lyons LA. Bach LH, et al. Among authors: lyons la. Cytogenet Genome Res. 2012;137(1):7-14. doi: 10.1159/000339416. Epub 2012 Jul 6. Cytogenet Genome Res. 2012. PMID: 22777158 Free PMC article.
202 results