Cargando…
A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder
In heterozygous females affected by an X-linked skin disorder, lesions often appear in a characteristic pattern, the so-called Blaschko’s lines. We investigated a female Labrador Retriever and her crossbred daughter, which both showed similar clinical lesions that followed Blaschko’s lines. The two...
Autores principales: | Bauer, Anina, De Lucia, Michela, Jagannathan, Vidhya, Mezzalira, Giorgia, Casal, Margret L., Welle, Monika M., Leeb, Tosso |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592936/ https://www.ncbi.nlm.nih.gov/pubmed/28739597 http://dx.doi.org/10.1534/g3.117.1124 |
Ejemplares similares
-
NSDHL Frameshift Deletion in a Mixed Breed Dog with Progressive Epidermal Nevi
por: Christen, Matthias, et al.
Publicado: (2020) -
ABHD5 frameshift deletion in Golden Retrievers with ichthyosis
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) -
Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK)
por: Bannoehr, Jeanette, et al.
Publicado: (2020) -
A COL11A2 Mutation in Labrador Retrievers with Mild Disproportionate Dwarfism
por: Frischknecht, Mirjam, et al.
Publicado: (2013)