A novel nonsense mutation in the human dystrophin gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference7 articles.
1. Point mutation in the human dystrophin gene: Identification through Western blot analysis
2. Premature chain termination mutation causing Duchenne muscular dystrophy
3. Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR
4. Detection of a nonsense mutation in the dystrophin gene by multiple SSCP
5. Point mutations in the dystrophin gene.
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1. Duchenne Muscular Dystrophy Gene therapy;Current Gene Therapy;2022-11-18
2. DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy;Clinical Genetics;2005-05-04
3. Automated sequence screening of the entire dystrophin cdna in Duchenne dystrophy: Point mutation detection;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2005
4. Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysis;American Journal of Medical Genetics;1998-11-02
5. Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts;Biochimie;1997-07
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