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- W2386831460 abstract "A patient with progressive muscular atrophy was assessed for the disease-associated genes by next-generation sequencing technology and exon trap and sequence analysis. The results of the investigation identified 399 genes, covering all exons in addition to 10 bp on either side, which are specific to 659 types of neuromuscular disorders, including hypotypes. Exon capture and sequence analysis revealed that the patient possessed two splice site mutations in the dysferlin (DYSF) gene, c.144+1G>A and c.342+1G>T, and the presence of the mutations was confirmed by Sanger sequencing. The patient's mother and sister were also assessed and confirmed to have mutations within the DYSF gene, the mother with c.342+1G>T and the sister with c.144+1G>A. The two splice site mutations in the DYSF gene, c.144+1G>A and c.342+1G>T, have not previously been reported. Therefore, exon capture and sequence analysis is able to rapidly and efficiently screen for genetic alterations in neuromuscular disorders." @default.
- W2386831460 created "2016-06-24" @default.
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- W2386831460 date "2016-05-11" @default.
- W2386831460 modified "2023-10-18" @default.
- W2386831460 title "Screening two mutations in the dysferlin gene by exon capture and sequence analysis: A case report" @default.
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- W2386831460 doi "https://doi.org/10.3892/etm.2016.3332" @default.
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