Skin exhibits of Dark Ronald XX are homozygous wild type at the Warmblood fragile foal syndrome causative missense variant position in lysyl hydroxylase gene PLOD1.
Abstract: No abstract available
Publication Date: 2020-06-17 PubMed ID: 32557718DOI: 10.1111/age.12972Google Scholar: Lookup
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- Journal Article
Cite This Article
APA
Zhang X, Hirschfeld M, Schafberg R, Swalve H, Brenig B.
(2020).
Skin exhibits of Dark Ronald XX are homozygous wild type at the Warmblood fragile foal syndrome causative missense variant position in lysyl hydroxylase gene PLOD1.
Anim Genet, 51(5), 838-840.
https://doi.org/10.1111/age.12972 Publication
Researcher Affiliations
- Institute of Veterinary Medicine, University of Goettingen, Göttingen, Germany.
- Institute of Veterinary Medicine, University of Goettingen, Göttingen, Germany.
- Department of Obstetrics and Gynecology, University Medical Center Freiburg, Freiburg, Germany.
- Natural Sciences Collections, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
- Institute of Agricultural and Nutritional Sciences, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
- Institute of Agricultural and Nutritional Sciences, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
- Institute of Veterinary Medicine, University of Goettingen, Göttingen, Germany.
MeSH Terms
- Animals
- Horse Diseases / genetics
- Horses
- Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase
- Skin / pathology
References
This article includes 11 references
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- Hegreberg G.A. et al. (1969) J Hered 60, 249-54.
- Witzig P. et al. (1984) Schweiz Arch Tierheilkd 126, 589-96.
- Helle O. & Nes N.N. (1972) Acta Vet Scand 13, 443-5.
- Solomons B. (1984) Equine Vet J 16, 541-2.
- Wobbe M. et al. (2019) https://www.vit.de/fileadmin/DE/Zuchtwertschaetzung/InformationsartikelWFFS.vit20190412.pdf, 1-4.
- Fages A. et al. (2019) Cell 177, 1419-35, e31.
- Untergasser A. et al. (2012) Nucleic Acids Res 40, e115.
- Metzger J. et al. (2020) Equine Vet J.
Citations
This article has been cited 4 times.- Todd ET, Fromentier A, Sutcliffe R, Running Horse Collin Y, Perdereau A, Aury JM, Èche C, Bouchez O, Donnadieu C, Wincker P, Kalbfleisch T, Petersen JL, Orlando L. Imputed genomes of historical horses provide insights into modern breeding.. iScience 2023 Jul 21;26(7):107104.
- Grillos AS, Roach JM, de Mestre AM, Foote AK, Kinglsey NB, Mienaltowski MJ, Bellone RR. First reported case of fragile foal syndrome type 1 in the Thoroughbred caused by PLOD1 c.2032G>A.. Equine Vet J 2022 Nov;54(6):1086-1093.
- Rowe Á, Flanagan S, Barry G, Katz LM, Lane EA, Duggan V. Warmblood fragile foal syndrome causative single nucleotide polymorphism frequency in horses in Ireland.. Ir Vet J 2021 Oct 18;74(1):27.
- Reiter S, Wallner B, Brem G, Haring E, Hoelzle L, Stefaniuk-Szmukier M, Długosz B, Piórkowska K, Ropka-Molik K, Malvick J, Penedo MCT, Bellone RR. Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States.. Genes (Basel) 2020 Dec 18;11(12).
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