A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy.
The polyneuropathy of juvenile Greyhound show dogs shows clinical similarities to the genetically heterogeneous Charcot-Marie-Tooth (CMT) disease in humans. The pedigrees containing affected dogs suggest monogenic autosomal recessive inheritance and all affected dogs trace back to a single male. Her...
Guardado en:
Autores principales: | Cord Drögemüller, Doreen Becker, Barbara Kessler, Elisabeth Kemter, Jens Tetens, Konrad Jurina, Karin Hultin Jäderlund, Annette Flagstad, Michele Perloski, Kerstin Lindblad-Toh, Kaspar Matiasek |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2010
|
Materias: | |
Acceso en línea: | https://doaj.org/article/aee1b8b7687f4344a91ddc9782545df0 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy.
por: Camilla S Bruun, et al.
Publicado: (2013) -
Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene.
por: Doreen Becker, et al.
Publicado: (2010) -
Independent polled mutations leading to complex gene expression differences in cattle.
por: Natalie Wiedemar, et al.
Publicado: (2014) -
A non-coding genomic duplication at the HMX1 locus is associated with crop ears in highland cattle.
por: Caroline Tina Koch, et al.
Publicado: (2013) -
<i>LAMA2</i> Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy
por: Matthias Christen, et al.
Publicado: (2021)