Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genotyping cattle for inherited congenital myoclonus and maple syrup urine disease.

Australian veterinary journal - 1 Nov 2002

Healy P J, Dennis J A, Windsor P A, Pierce K D, Schofield P A

Abstract excerpt

OBJECTIVE: To develop a routine procedure for establishing the inherited congenital myoclonus (ICM) genotype of cattle and to obtain an estimate of the prevalence of heterozygotes for ICM and maple syrup urine disease (MSUD) in Australian Poll Herefords. DESIGN: A mismatch amplification procedure...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Australia
Share to Cattle
Share to Cattle Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Carrier Screening

Share to Incidence

Share to Maple Syrup Urine Disease

Share to Myoclonus

Share to Prevalence

Source

Identifiers

PMID: 12465829
DOI: 10.1111/j.1751-0813.2002.tb11301.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12465829-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotyping cattle for inherited congenital myoclonus and maple syrup urine disease.PMID 12465829Read ↗

Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles.Semantic proximity Read ↗

Heterozygote detection for maple syrup urine disease in cattle.Semantic proximity Read ↗

Molecular heterogeneity for bovine maple syrup urine disease.Semantic proximity Read ↗

A novel mutation of the CLCN1 gene associated with myotonia hereditaria in an Australian cattle dog.Semantic proximity Read ↗

A clinical case of CACNA1S-related muscle weakness in a Holstein calf with congenital astasia diagnosed by a genotyping test of stored blood.Semantic proximity Read ↗

Congenital myasthenic syndrome of Brahman cattle in South Africa.Semantic proximity Read ↗

Lethal genetic disorder in Poll Merino/Merino sheep in Australia.Semantic proximity Read ↗

Diagnostic assay for the causative allele for Jersey Neuropathy with Splayed Forelimbs.Semantic proximity Read ↗

The CHRNE 470del20 mutation causing congenital myasthenic syndrome in South African Brahman cattle: prevalence, origin, and association with performance traits.Semantic proximity Read ↗

Use of hair root as a source of DNA for the detection of heterozygotes for recessive defects in cattle.Semantic proximity Read ↗

Genetic test for myophosphorylase deficiency in Charolais cattle.Semantic proximity Read ↗

Genotyping Brahman cattle for generalised glycogenosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.