Allele Frequency of APAF1 Mutation in Holstein Cattle in Brazil

APAF1 is an autosomal recessive inherited mutation, associated with Holstein haplotype 1 (HH1) and characterized by a substitution of cytosine for a thymine (c.1741C>T) in chromosome 5. The mutation causes fetal and embryonic loss, between 60 and 200 days of gestation, and reduced conception rate...

Descripción completa

Detalles Bibliográficos
Autores principales: Albertino, Lukas Garrido, Albuquerque, Ana Luísa Holanda, Ferreira, Julia Franco, Oliveira, João Pedro Marmol, Borges, Alexandre Secorun, Patelli, Thais Helena Constantino, Oliveira-Filho, José Paes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Veterinary Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904897/
https://www.ncbi.nlm.nih.gov/pubmed/35280144
http://dx.doi.org/10.3389/fvets.2022.822224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904897/
https://www.ncbi.nlm.nih.gov/pubmed/35280144
http://dx.doi.org/10.3389/fvets.2022.822224

Ejemplares similares