Cargando…
Feline Cystinuria Caused by a Missense Mutation in the SLC3A1 Gene
BACKGROUND: Cystinuria is an inherited metabolic disease that is relatively common in dogs, but rare in cats and is characterized by defective amino acid reabsorption, leading to cystine urolithiasis. OBJECTIVES: The aim of this study was to report on a mutation in a cystinuric cat. ANIMALS: A male...
Autores principales: | Mizukami, K., Raj, K., Giger, U. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858075/ https://www.ncbi.nlm.nih.gov/pubmed/25417848 http://dx.doi.org/10.1111/jvim.12501 |
Ejemplares similares
-
Cystinuria Associated with Different SLC7A9 Gene Variants in the Cat
por: Mizukami, Keijiro, et al.
Publicado: (2016) -
Pediatric Cystinuria Patient With Novel Mutation in
SLC3A1
por: Watanabe, Yoshitaka, et al.
Publicado: (2019) -
Clinical Characteristics and In Silico Analysis of Cystinuria Caused by a Novel SLC3A1 Mutation
por: Liu, Lexin, et al.
Publicado: (2022) -
Cystinuria in a 13-month-old Girl with Absence of Mutations in the SLC3A1 and SLC7A9 Genes
por: Krishnamurthy, S., et al.
Publicado: (2018) -
DEA 1 Expression on Dog Erythrocytes Analyzed by Immunochromatographic and Flow Cytometric Techniques
por: Acierno, M.M., et al.
Publicado: (2014)