A MITF Mutation Associated with a Dominant White Phenotype and Bilateral Deafness in German Fleckvieh Cattle

A dominantly inherited syndrome associated with hypopigmentation, heterochromia irides, colobomatous eyes and bilateral hearing loss has been ascertained in Fleckvieh cattle (German White Fleckvieh syndrome). This syndrome has been mapped to bovine chromosome (BTA) 22 using a genome-wide association...

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Detalles Bibliográficos
Autores principales: Philipp, Ute, Lupp, Bettina, Mömke, Stefanie, Stein, Veronika, Tipold, Andrea, Eule, Johanna Corinna, Rehage, Jürgen, Distl, Ottmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236222/
https://www.ncbi.nlm.nih.gov/pubmed/22174915
http://dx.doi.org/10.1371/journal.pone.0028857

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236222/
https://www.ncbi.nlm.nih.gov/pubmed/22174915
http://dx.doi.org/10.1371/journal.pone.0028857

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