Familiar Hypopigmentation Syndrome in Sheep Associated with Homozygous Deletion of the Entire Endothelin Type-B Receptor Gene

In humans, rodents and horses, pigmentary anomalies in combination with other disorders, notably intestinal aganglionosis, are associated with variants of the endothelin type-B receptor gene (EDNRB). In an inbred Cameroon sheep flock, five white lambs with light blue eyes were sired from the same ra...

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Detalles Bibliográficos
Autores principales: Lühken, Gesine, Fleck, Katharina, Pauciullo, Alfredo, Huisinga, Maike, Erhardt, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534075/
https://www.ncbi.nlm.nih.gov/pubmed/23300849
http://dx.doi.org/10.1371/journal.pone.0053020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534075/
https://www.ncbi.nlm.nih.gov/pubmed/23300849
http://dx.doi.org/10.1371/journal.pone.0053020

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