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A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy.
Letko A, Minor KM, Friedenberg SG, Shelton GD, Salvador JP, Mandigers PJJ, Leegwater PAJ, Winkler PA, Petersen-Jones SM, Stanley BJ, Ekenstedt KJ, Johnson GS, Hansen L, Jagannathan V, Mickelson JR, Drögemüller C. Letko A, et al. Among authors: leegwater paj. Genes (Basel). 2020 Nov 27;11(12):1426. doi: 10.3390/genes11121426. Genes (Basel). 2020. PMID: 33261176 Free PMC article.
COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy.
Gandolfi B, Grahn RA, Creighton EK, Williams DC, Dickinson PJ, Sturges BK, Guo LT, Shelton GD, Leegwater PA, Longeri M, Malik R, Lyons LA. Gandolfi B, et al. Anim Genet. 2015 Dec;46(6):711-5. doi: 10.1111/age.12350. Epub 2015 Sep 16. Anim Genet. 2015. PMID: 26374066 Free PMC article.
Canine NAPEPLD-associated models of human myelin disorders.
Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C. Minor KM, et al. Among authors: leegwater paj. Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7. Sci Rep. 2018. PMID: 29643404 Free PMC article.
111 results