Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference43 articles.
1. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide
2. Prenatal diagnosis of Duchenne muscular dystrophy: A three-year experience in a rapidly evolving field
3. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies
4. Improved diagnosis of Duchenne/Becker muscular dystrophy.
5. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
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2. Análisis del espectro mutacional de la distrofia muscular de Duchenne en un grupo de pacientes colombianos;Neurología Argentina;2018-07
3. Germinal Mosaicism in a Sample of Families with Duchenne/Becker Muscular Dystrophy with Partial Deletions in the DMD Gene;Genetic Testing and Molecular Biomarkers;2014-02
4. Intragenic DNA Polymorphism Analysis of DMD/BMD Dystrophy Gene for Carrier and Prenatal Diagnosis in 60 Iranian Healthy Individuals;International Journal of Neuroscience;2011-07-21
5. Deletional mutations of dystrophin gene and carrier detection in eastern India;The Indian Journal of Pediatrics;2009-10
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