Ruling out BGN variants as simple X-linked causative mutations for bilateral corneal stromal loss in Friesian horses
Anim Genet
.
2018 Dec;49(6):656-657.
doi: 10.1111/age.12726.
Epub 2018 Sep 23.
Authors
Coral Alberi
1
2
,
Erin Hisey
1
2
,
Mary Lassaline
3
,
Alyssa Atilano
1
2
,
Theodore Kalbfleisch
4
,
Riccardo Stoppini
5
,
Hanneke Hermans
6
,
Willem Back
6
,
Michael J Mienaltowski
7
,
Rebecca R Bellone
1
2
Affiliations
1
Department of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA, 95616, USA.
2
Veterinary Genetics Laboratory, School of Veterinary Medicine, University of California-Davis, Davis, CA, 95616, USA.
3
Department of Surgical & Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, CA, 95616, USA.
4
Biochemistry and Molecular Biology, School of Medicine, University of Louisville, Louisville, KY, 402925, USA.
5
Clinica Veterinaria Equina Cascina Gufa, Strada Provinciale 201 Km 3, 26833, Merlino, LO, Italy.
6
Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 112-114, NL-3584 CM, Utrecht, The Netherlands.
7
Department of Animal Science, College of Agricultural and Environmental Sciences, University of California-Davis, Davis, CA, 95616, USA.
PMID:
30246344
DOI:
10.1111/age.12726
No abstract available
MeSH terms
Animals
Biglycan / genetics*
Corneal Dystrophies, Hereditary / genetics
Corneal Dystrophies, Hereditary / veterinary*
Genes, X-Linked*
Horse Diseases / genetics*
Horses
Substances
Biglycan
Grants and funding
D16EQ-820/Morris Animal Foundation