Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference22 articles.
1. Pharmacologic management of Duchenne muscular dystrophy: target identification and clinical trials;Kornegay;ILAR J,2014
2. X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterization;Barthélémy;Skelet Muscle,2020
3. Muscular dystrophy in a dog resembling human Becker muscular dystrophy;Baroncelli;J Comp Pathol,2014
4. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype;Vieira;Neuromuscul Disord,2015
5. Independent canine models of Duchenne muscular dystrophy due to intronic insertions of repetitive DNA;Smith;Mol Ther,2007
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3. Whole Animal Genome Sequencing: user-friendly, rapid, containerized pipelines for processing, variant discovery, and annotation of short-read whole genome sequencing data;G3: Genes, Genomes, Genetics;2023-05-27
4. Advances in CRISPR/Cas9 Genome Editing for the Treatment of Muscular Dystrophies;Human Gene Therapy;2023-05-01
5. Dystrophin (DMD) Missense Variant in Cats with Becker-Type Muscular Dystrophy;International Journal of Molecular Sciences;2023-02-06
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