ArticleVeterinary and animal science2026
Novel
Article in Veterinary and animal science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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0 citing papers in PubMed.
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Authors and funding
7 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Genetic neuromuscular disorders (NMDs) are characterized by progressive skeletal muscle degeneration and weakness. In Brown Swiss (BS) cattle, three recessive variants have been associated with NMDs. This study aimed to (1) describe the phenotype of BS cattle affected by a novel form of postural proprioceptive deficits, (2) identify a candidate genetic variant using whole-genome sequencing (WGS), and (3) estimate its prevalence in the Swiss BS population. A first BS heifer (case 1) showing ataxia underwent clinical and hematological examination, followed by WGS of the heifer and its sire. Variants were filtered and compared against 5577 controls. Candidate variants were evaluated
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.