A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle

Genodermatosis such as hair disorders mostly follow a monogenic mode of inheritance. Congenital hypotrichosis (HY) belong to this group of disorders and is characterized by abnormally reduced hair since birth. The purpose of this study was to characterize the clinical phenotype of a breed-specific n...

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Detalles Bibliográficos
Autores principales: Kuca, Thibaud, Marron, Brandy M., Jacinto, Joana G. P., Paris, Julia M., Gerspach, Christian, Beever, Jonathan E., Drögemüller, Cord
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147104/
https://www.ncbi.nlm.nih.gov/pubmed/33926013
http://dx.doi.org/10.3390/genes12050643

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147104/
https://www.ncbi.nlm.nih.gov/pubmed/33926013
http://dx.doi.org/10.3390/genes12050643

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