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Evaluation of Exon Inclusion Induced by Splice Switching Antisense Oligonucleotides in SMA Patient Fibroblasts
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Author response: Discrepancy in redetermination of SMN2 copy numbers in children with SMA

Janbernd Kirschner1, Jutta Becker2, David Schorling3

  • 1(Bonn, Germany).

Neurology
|July 22, 2020
PubMed
Abstract

No abstract available in PubMed .

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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