Multi-exon genotyping of SMN gene in spinal muscular atrophy by universal fluorescent PCR and capillary electrophoresis
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,Analytical Chemistry
Reference37 articles.
1. De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies
2. 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
3. Genetic testing and risk assessment for spinal muscular atrophy (SMA)
4. Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling
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1. Comprehensive Analysis of Spinal Muscular Atrophy;The Journal of Molecular Diagnostics;2022-09
2. The phospho-landscape of the survival of motoneuron protein (SMN) protein: relevance for spinal muscular atrophy (SMA);Cellular and Molecular Life Sciences;2022-08-25
3. Revealing diverse alternative splicing variants of the highly homologous SMN1 and SMN2 genes by targeted long-read sequencing;Molecular Genetics and Genomics;2022-05-25
4. Identifiable universal fluorescent multiplex PCR equipped with capillary electrophoresis for genotyping of exons 1 to 5 in human red and green pigment genes;Talanta;2022-05
5. Genomic Variability in the Survival Motor Neuron Genes (SMN1 and SMN2): Implications for Spinal Muscular Atrophy Phenotype and Therapeutics Development;International Journal of Molecular Sciences;2021-07-23
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