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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...

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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

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