Skin exhibits of Dark Ronald XX are homozygous wild type at the Warmblood fragile foal syndrome causative missense variant position in lysyl hydroxylase genePLOD1-Reference-Cited by-同舟云学术

Skin exhibits of Dark Ronald XX are homozygous wild type at the Warmblood fragile foal syndrome causative missense variant position in lysyl hydroxylase genePLOD1

Published:2020-06-17 Issue:5 Volume:51 Page:838-840
ISSN:0268-9146
Container-title:Animal Genetics
language:en
Short-container-title:Anim Genet

Author:

Zhang Xuying¹,Hirschfeld Marc¹²,Schafberg Renate³⁴,Swalve Hermann⁴,Brenig Bertram¹^ORCID

Affiliation:

1. Institute of Veterinary Medicine University of Goettingen Göttingen Germany

2. Department of Obstetrics and Gynecology University Medical Center Freiburg Freiburg Germany

3. Natural Sciences Collections Martin‐Luther‐University Halle‐Wittenberg Halle (Saale) Germany

4. Institute of Agricultural and Nutritional Sciences Martin‐Luther‐University Halle‐Wittenberg Halle (Saale) Germany

Publisher

Wiley

Subject

Genetics,Animal Science and Zoology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/age.12972

Reference11 articles.

1. DANLOS SYNDROME ASSOCIATED WITH CONGENITAL LIPOMATOSIS

2. A case of Ehlers‐Danlos‐like syndrome in a rabbit with a review of the disease in other species

3. A Connective Tissue Disease of Dogs and Mink Resembling the Ehlers-Danlos Syndrome of Man

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1. Imputed genomes of historical horses provide insights into modern breeding;iScience;2023-07

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3. Warmblood fragile foal syndrome causative single nucleotide polymorphism frequency in horses in Ireland;Irish Veterinary Journal;2021-10-18

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5. 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;2020-12-18