Two Non-Contiguous Duplications in theDMDGene in a Spanish Family
Author:
Publisher
Informa UK Limited
Subject
Cellular and Molecular Neuroscience,Genetics
Link
http://www.tandfonline.com/doi/pdf/10.1080/01677060701686184
Reference21 articles.
1. Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
2. An alternative dystrophin transcript specific to peripheral nerve
3. Restoration of half the normal dystrophin sequence in a double-deletion Duchenne muscular dystrophy family
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1. Prenatal risk assessment of Xp21.1 duplication involving theDMDgene by optical genome mapping;Life Science Alliance;2024-08-08
2. Uncovering the true features of dystrophin gene rearrangement and improving the molecular diagnosis of Duchenne and Becker muscular dystrophies;iScience;2023-12
3. Captured long-read sequecing provides an efficient and accurate method for molecular diagnosis of Duchenne and Becker muscular dystrophies;2022-12-02
4. Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation;Neurological Sciences;2015-06-17
5. Novel Non-contiguous Duplications in theDMDGene in Five Patients with Duchenne Muscular Dystrophy;Laboratory Medicine Online;2015
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