Molecular Basis of Inherited Diseases in Companion Animals 

<br/><br/><br/>English[eng] 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Canis familiaris||dermatology||immunology||animal model||skin||TLR7||toll-like receptor||syndecan binding protein||syntenin-1||systemic lupus erythematosus||SLE||CLE||whole-genome sequencing||craniomandibular osteopathy||calvarial hyperostotic syndrome||Caffey disease||infantile cortical hyperostosis||rare disease||SLC37A2||COL1A1||SLC35D1||Canis lupus familiaris||whole-genome sequence||genodermatosis||keratinocyte||SAM syndrome||precision medicine||dog||desmosome||acantholysis||calcium||veterinary medicine||feline||Felis catus||brain malformation||BMP12||neurodevelopment||genetics||genomics||mendelian traits||genome-wide association study||whole genome sequencing||mitochondrion||phosphoenolpyruvate-carboxykinase||inborn error of metabolism||encephalopathy||SSADHD||ALDH5A1||GABA||4-hydroxybutyric acid||succinic semialdehyde||GWAS||inherited||whole genome sequence||wgs||laminin||Bardet–Biedl syndrome (BBS)||primary cilia||ciliopathy||BBS8||progressive retinal atrophy (PRA)||retinitis pigmentosa||canine||dystrophinopathy||Duchenne||immunohistochemistry||neurometabolic disorder||CHILD syndrome||ILVEN||epidermal nevus||diabetes mellitus||Burmese cats||susceptibility||single-nucleotide polymorphism||genetic markers||LIPH||obesity||companion animals||metabolic disease||comparative genomics||dogs||cats||horses||contactin||neurological disorder||Leonberger||Saint Bernard||Labrador retriever||n/a