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Animal Genetics|November 13, 2010
Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breedsM E McCue, S M Anderson, S J Valberg, et al.
Infection and Immunity|April 7, 1998
Characterization of leptospiral outer membrane lipoprotein LipL36: downregulation associated with late-log-phase growth and mammalian infectionD A Haake, C Martinich, T A Summers, et al.
Scientific Reports|November 1, 2019
A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigsC E T Araújo, C M C Oliveira, J D Barbosa, et al.
Scientific Reports|February 27, 2020
Publisher Correction: A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigsC E T Araújo, C M C Oliveira, J D Barbosa, et al.
Biochimica Et Biophysica Acta. General Subjects|September 5, 2016
A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthaseC A Maile, J R Hingst, K K Mahalingan, et al.
BMC Genomics|December 1, 2020
Whole genome sequencing identified a 16 kilobase deletion on ECA13 associated with distichiasis in Friesian horsesE A Hisey, H Hermans, Z T Lounsberry, et al.
Animal Genetics|January 29, 2014
Genetic risk factors for insidious equine recurrent uveitis in Appaloosa horsesK L Fritz, H J Kaese, S J Valberg, et al.
Animal Genetics|September 18, 2025
IMAGE001: A new livestock multispecies SNP array to characterize genomic variation in European livestock gene bank collectionsR P M A Crooijmans, R Gonzalez Prendes, L Colli, et al.
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