Cargando…
Microphthalmia in Texel Sheep Is Associated with a Missense Mutation in the Paired-Like Homeodomain 3 (PITX3) Gene
Microphthalmia in sheep is an autosomal recessive inherited congenital anomaly found within the Texel breed. It is characterized by extremely small or absent eyes and affected lambs are absolutely blind. For the first time, we use a genome-wide ovine SNP array for positional cloning of a Mendelian t...
Autores principales: | Becker, Doreen, Tetens, Jens, Brunner, Adrian, Bürstel, Daniela, Ganter, Martin, Kijas, James, Drögemüller, Cord |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805710/ https://www.ncbi.nlm.nih.gov/pubmed/20084168 http://dx.doi.org/10.1371/journal.pone.0008689 |
Ejemplares similares
-
Anatomy and Pathology of the Texel Sheep Larynx
por: Waine, Katie, et al.
Publicado: (2019) -
Flock health survey of Irish Texel society breeders and larynx examination in Texel sheep
por: Kennedy, Aideen, et al.
Publicado: (2020) -
Expression of Truncated PITX3 in the Developing Lens Leads to Microphthalmia and Aphakia in Mice
por: Wada, Kenta, et al.
Publicado: (2014) -
Functional analysis of human mutations in homeodomain transcription factor PITX3
por: Sakazume, Satoru, et al.
Publicado: (2007) -
Genome-wide association study of footrot in Texel sheep
por: Mucha, Sebastian, et al.
Publicado: (2015)