Cargando…
Congenital muscular dystrophy in a dog with a LAMA2 gene deletion
A 2‐year‐old female spayed dog was presented with a chronic history of short‐strided gait and inability to completely open the jaw. Clinical signs were present since the dog was adopted from a humane society at a few months of age. Serum creatine kinase activity was abnormally high. Neurological exa...
Autores principales: | Shelton, G. Diane, Minor, Katie M., Thomovsky, Stephanie, Guo, Ling T., Friedenberg, Steven G., Cullen, Jonah N., Mickelson, James R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783360/ https://www.ncbi.nlm.nih.gov/pubmed/34854126 http://dx.doi.org/10.1111/jvim.16330 |
Ejemplares similares
-
Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich‐like congenital muscular dystrophy
por: Jankelunas, Leanne, et al.
Publicado: (2023) -
Current Classification of Canine Muscular Dystrophies and Identification of New Variants
por: Shelton, G. Diane, et al.
Publicado: (2023) -
Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D
por: Mickelson, James R., et al.
Publicado: (2021) -
Targeted sequencing of candidate gene regions for myelofibrosis in dogs
por: Campbell, Amelia G., et al.
Publicado: (2022) -
LAMA2 Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy
por: Christen, Matthias, et al.
Publicado: (2021)