Carbamazepine treatment of myotonia congenita in a cat by Genesis V Lopez Bonilla, Elizabeth Parsley, G Diane Shelton, Dominik Faissler

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Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X‐linked muscular dystrophy in a cat by G. Diane Shelton, Fabrizio Tucciarone, Ling T. Guo, Lyndon M. Coghill, Leslie A. Lyons

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Feline dystrophin-deficient muscular dystrophy misdiagnosed as myositis by Rachel M Reynolds, Stanley L Marks, Ling T Guo, G. Diane Shelton, Karina J Graham

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Long‐term outcome of Miniature Schnauzers with genetically confirmed demyelinating polyneuropathy: 12 cases by Alba Farré Mariné, Nicolas Granger, Coralie Bertolani, Joan Mascort Boixeda, G. Diane Shelton, Alejandro Luján Feliu‐Pascual

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Pathologic Changes in and Immunophenotyping of Polymyositis in the Dutch Kooiker Dog by Vanessa Alf, Yvet Opmeer, G. Diane Shelton, Guy C. M. Grinwis, Kaspar Matiasek, Marco Rosati, Paul J. J. Mandigers

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Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia by G. Diane Shelton, James R. Mickelson, Steven G. Friedenberg, Jonah N. Cullen, Jaya M. Mehra, Ling T. Guo, Katie M. Minor

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A Nonsense Variant in the <i>DMD</i> Gene Causes X-Linked Muscular Dystrophy in the Maine Coon Cat by Evy Beckers, Ine Cornelis, Sofie F. M. Bhatti, Pascale Smets, G. Diane Shelton, Ling T. Guo, Luc Peelman, Bart J. G. Broeckx

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Variants in <i>CLCN1</i> and <i>PDE4C</i> Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs by G. Diane Shelton, James R. Mickelson, Steven G. Friedenberg, Jonah N. Cullen, Karina Graham, Missy C. Carpentier, Ling T. Guo, Katie M. Minor

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NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model by Matthias Christen, Anne Gregor, Rodrigo Gutierrez-Quintana, Jos Bongers, Angie Rupp, Jacques Penderis, G. Diane Shelton, Vidhya Jagannathan, Christiane Zweier, Tosso Leeb

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An Inflammatory Myopathy in the Dutch Kooiker Dog by Yvet Opmeer, Guy C. M. Grinwis, G. Diane Shelton, Marco Rosati, Vanessa Alf, Hille Fieten, Peter A. J. Leegwater, Kaspar Matiasek, Paul J. J. Mandigers

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Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich‐like congenital muscular dystrophy by Leanne Jankelunas, Vishal D. Murthy, Annie V. Chen, Katie M. Minor, Steven G. Friedenberg, Jonah N. Cullen, Ling T. Guo, James R. Mickelson, G. Diane Shelton

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An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. by Kari J Ekenstedt, Doreen Becker, Katie M Minor, G Diane Shelton, Edward E Patterson, Tim Bley, Anna Oevermann, Thomas Bilzer, Tosso Leeb, Cord Drögemüller, James R Mickelson

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Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation by Kate L. Tsai, Karen M. Vernau, Kathryn Winger, Danielle M. Zwueste, Beverly K. Sturges, Marguerite Knipe, D. Colette Williams, Kendall J. Anderson, Jacquelyn M. Evans, Ling T. Guo, Leigh Anne Clark, G. Diane Shelton

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X‐linked myotubular myopathy associated with an MTM1 variant in a Maine coon cat by Matthew A. Kopke, G. Diane Shelton, Leslie A. Lyons, Meredith J. Wall, Sarah Pemberton, Kristene R. Gedye, Rebecca Owen, Ling T. Guo, Reuben M. Buckley, Juan A. Valencia, 99 Lives Consortium, Boyd R. Jones

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Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. by Karen M Vernau, Jonathan A Runstadler, Emily A Brown, Jessie M Cameron, Heather J Huson, Robert J Higgins, Cameron Ackerley, Beverly K Sturges, Peter J Dickinson, Birgit Puschner, Cecilia Giulivi, G Diane Shelton, Brian H Robinson, Salvatore DiMauro, Andrew W Bollen, Danika L Bannasch

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