Wikidata

(Q84970421)

English

A rare SMN2 variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy

scientific article published on 01 January 2010

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title
A rare SMN2 variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
19953646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19953646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 February 2020
author name string

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