Literature DB >> 32557718

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.

Xuying Zhang1, Marc Hirschfeld1,2, Renate Schafberg3,4, Hermann Swalve4, Bertram Brenig1.   

Abstract

Entities:  

Year:  2020        PMID： 32557718     DOI： 10.1111/age.12972

Source DB:  PubMed          Journal:  Anim Genet        ISSN： 0268-9146            Impact factor:   3.169


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  2 in total

1.  First reported case of fragile foal syndrome type 1 in the Thoroughbred caused by PLOD1 c.2032G>A.

Authors:  Alexandra S Grillos; Jessica M Roach; Amanda M de Mestre; Alastair K Foote; Nicole B Kinglsey; Michael J Mienaltowski; Rebecca R Bellone
Journal:  Equine Vet J       Date:  2022-02-01       Impact factor: 2.692

2.  Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States.

Authors:  Simone Reiter; Barbara Wallner; Gottfried Brem; Elisabeth Haring; Ludwig Hoelzle; Monika Stefaniuk-Szmukier; Bogusława Długosz; Katarzyna Piórkowska; Katarzyna Ropka-Molik; Julia Malvick; Maria Cecilia T Penedo; Rebecca R Bellone
Journal:  Genes (Basel)       Date:  2020-12-18       Impact factor: 4.096
  2 in total

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