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A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
BACKGROUND: Haplotypes with reduced or missing homozygosity may harbor deleterious alleles that compromise juvenile survival. A scan for homozygous haplotype deficiency revealed a short segment on bovine chromosome 19 (Braunvieh haplotype 2, BH2) that was associated with high juvenile mortality in B...
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Publicado no: | BMC Genomics |
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Main Authors: | , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4880872/ https://ncbi.nlm.nih.gov/pubmed/27225349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-016-2742-y |
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