Showing 1 - 9 results of 9 for search 'Mhlanga-Mutangadura, T', query time: 0.04s
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Neuronal ceroid lipofuscinosis in a German Shorthaired Pointer associated with a previously reported CLN8 nonsense variant by Juyuan Guo, Gary S. Johnson, James Cook, Olivia K. Harris, Tendai Mhlanga-Mutangadura, Robert D. Schnabel, Cheryl A. Jensen, Martin L. Katz
Published 2019-12-01
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A Homozygous <i>MAN2B1</i> Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficie... by Garrett Bullock, Gary S. Johnson, Savannah G. Pattridge, Tendai Mhlanga-Mutangadura, Juyuan Guo, James Cook, Rebecca S. Campbell, Charles H. Vite, Martin L. Katz
Published 2023-08-01
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Homozygous <i>CNP</i> Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions by Stefan H. Keller, Gary S. Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Savannah G. Pattridge, Juyuan Guo, Gregg D. Kortz, Martin L. Katz
Published 2024-02-01
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A Homozygous KCNJ10 Mutation in Jack Russell Terriers and Related Breeds with Spinocerebellar Ataxia with Myokymia, Seizures, or Both by D. Gilliam, D.P. O'Brien, J.R. Coates, G.S. Johnson, G.C. Johnson, T. Mhlanga‐Mutangadura, L. Hansen, J.F. Taylor, R.D. Schnabel
Published 2014-05-01
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Exploring genetic variation and population structure in a threatened species, <i>Noturus placidus</i>, with whole-genome sequence data by Lynsey K Whitacre, Mark L Wildhaber, Gary S Johnson, Harly J Durbin, Troy N Rowan, Peoria Tribe, Robert D Schnabel, Tendai Mhlanga-Mutangadura, Vernon M Tabor, Daniel Fenner, Jared E Decker
Published 2022-02-01
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Novel Homozygous <i>ADAMTS2</i> Variants and Associated Disease Phenotypes in Dogs with Dermatosparactic Ehlers–Danlos Syndrome by Jared A. Jaffey, Garrett Bullock, Juyuan Guo, Tendai Mhlanga-Mutangadura, Dennis P. O’Brien, Joan R. Coates, Rochelle Morrissey, Robert Hutchison, Kevin S. Donnelly, Leah A. Cohn, Martin L. Katz, Gary S. Johnson
Published 2022-11-01
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A mutation in the Warburg syndrome gene, RAB3GAP1, causes a similar syndrome with polyneuropathy and neuronal vacuolation in Black Russian Terrier dogs by Tendai Mhlanga-Mutangadura, Gary S. Johnson, Robert D. Schnabel, Jeremy F. Taylor, Gayle C. Johnson, Martin L. Katz, G. Diane Shelton, Teresa E. Lever, Elizabeth Giuliano, Nicolas Granger, Jeremy Shomper, Dennis P. O'Brien
Published 2016-02-01
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Characterization of genetic and phenotypic diversity of invasive nontypeable Haemophilus influenzae. by Erwin, A, Nelson, K, Mhlanga-Mutangadura, T, Bonthuis, P, Geelhood, J, Morlin, G, Unrath, W, Campos, J, Crook, D, Farley, M, Henderson, F, Jacobs, R, Mühlemann, K, Satola, S, van Alphen, L, Golomb, M, Smith, A
Published 2005Journal article