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A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy

Crossref DOI link: https://doi.org/10.1038/ejhg.2015.213

Published Online: 2015-09-30

Published Print: 2016-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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