Cargando…
SOAT1 missense variant in two cats with sebaceous gland dysplasia
Spontaneously arisen hereditary diseases in domestic animals provide an excellent opportunity to study the physiological functions of the altered genes. We investigated two 4-month-old sibling domestic short haired kittens with dry dark debris around the eyes, nose, and ears, dark crusting on the le...
Autores principales: | Kiener, Sarah, McMahill, Barbara G., Affolter, Verena K., Welle, Monika, Yager, Julie A., Jagannathan, Vidhya, Leeb, Tosso |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227112/ https://www.ncbi.nlm.nih.gov/pubmed/37060467 http://dx.doi.org/10.1007/s00438-023-02020-6 |
Ejemplares similares
-
A Missense Variant in SLC39A4 in a Litter of Turkish Van Cats with Acrodermatitis Enteropathica
por: Kiener, Sarah, et al.
Publicado: (2021) -
Independent DSG4 frameshift variants in cats with hair shaft dystrophy
por: Kiener, Sarah, et al.
Publicado: (2021) -
A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis
por: Affolter, Verena K., et al.
Publicado: (2022) -
A TAC3 Missense Variant in a Domestic Shorthair Cat with Testicular Hypoplasia and Persistent Primary Dentition
por: Hug, Petra, et al.
Publicado: (2019) -
Dystrophin (DMD) Missense Variant in Cats with Becker-Type Muscular Dystrophy
por: Hilton, Stephanie, et al.
Publicado: (2023)