Universal multiplex PCR and CE for quantification ofSMN1/SMN2genes in spinal muscular atrophy
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,Analytical Chemistry
Reference28 articles.
1. Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy
2. De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies
3. Natural History in Proximal Spinal Muscular Atrophy
4. A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2
5. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)
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1. Exon7 Targeted CRISPR-Prime Editing Approaches for SMN2 Gene Editing in Spinal Muscular Atrophy (SMA) Disease Can Increase In Vitro SMN Expression;2022-03-21
2. Molecular inversion probes equipped with discontinuous rolling cycle amplification for targeting nucleotide variants: Determining SMN1 and SMN2 genes in diagnosis of spinal muscular atrophy;Analytica Chimica Acta;2017-07
3. Evaluation and characterization of a high-resolution melting analysis kit for rapid carrier-screening test of spinal muscular atrophy;Journal of Neurogenetics;2015-04-20
4. SMA prenatal diagnosis: A modified protocol to help differentiation between deletions and gene conversion;Molecular and Cellular Probes;2015-02
5. Genotyping of intron 22 inversion of factor VIII gene for diagnosis of hemophilia A by inverse-shifting polymerase chain reaction and capillary electrophoresis;Analytical and Bioanalytical Chemistry;2014-07-04
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