Discover Community Create You

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

Investigation of Known Genetic Mutations of Arabian Horses in Egyptian Arabian Foals with Juvenile Idiopathic Epilepsy.

Journal of veterinary internal medicine - 1 Jan 2018

Aleman M, Finno C J, Weich K, Penedo M C T

Abstract excerpt

BACKGROUND: The carrier status of lavender foal syndrome (LFS), cerebellar abiotrophy (CA), severe combined immunodeficiency (SCID), and occipitoatlantoaxial malformation (OAAM1) in foals with juvenile idiopathic epilepsy (JIE) is unknown. HYPOTHESIS/OBJECTIVES: To determine the carrier status of LFS, CA, SCID, and OAAM1 in foals with JIE. ANIMALS: Ten foals with JIE. MATERIALS AND METHODS: Archived DNA samples...

Read the complete abstract on PubMed

Topics

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

Share to Epilepsy
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Heterozygote

Share to Horse Diseases

Share to Horses

Source

Open in PubMed Open full text

Identifiers

PMID: 29171123
DOI: 10.1111/jvim.14873
PMCID: PMC5787150

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Investigation of Known Genetic Mutations of Arabian Horses in Egyptian Arabian Foals with Juvenile Idiopathic Epilepsy.PMID 29171123Read ↗

Investigation of Cerebellar Abiotrophy (CA), Lavender Foal Syndrome (LFS), and Severe Combined Immunodeficiency (SCID) Variants in a Cohort of Three MENA Region Horse Breeds.Semantic proximity Read ↗

The carrier prevalence of severe combined immunodeficiency, lavender foal syndrome and cerebellar abiotrophy in Arabian horses in South Africa.Semantic proximity Read ↗

Inheritance of cerebellar abiotrophy in Arabians.Semantic proximity Read ↗

The frequency of the equine cerebellar abiotrophy mutation in non-Arabian horse breeds.Semantic proximity Read ↗

Juvenile idiopathic epilepsy in Egyptian Arabian foals: 22 cases (1985-2005).Semantic proximity Read ↗

Evidence for origin of lavender foal syndrome among Egyptian Arabian horses in Egypt.Semantic proximity Read ↗

Role of KCNQ2 and KCNQ3 genes in juvenile idiopathic epilepsy in Arabian foals.Semantic proximity Read ↗

Morphometric magnetic resonance imaging and genetic testing in cerebellar abiotrophy in Arabian horses.Semantic proximity Read ↗

An inherited SLC25A12-related recessive form of congenital porencephaly in Limousin cattle.Semantic proximity Read ↗

Genetic Testing as a Tool to Identify Horses with or at Risk for Ocular Disorders.Semantic proximity Read ↗

Variation in MUTYH expression in Arabian horses with Cerebellar Abiotrophy.Semantic proximity Read ↗

Defining Trends in Global Gene Expression in Arabian Horses with Cerebellar Abiotrophy.Semantic proximity Read ↗

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