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EJHG.2015.213
EJHG.2015.213
http://dx.doi.org/10.1038/EJHG.2015.213
A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy
P356
Q36902715-92815886-C7C0-4995-8279-E1DDEB429FA3
P356
EJHG.2015.213
http://dx.doi.org/10.1038/EJHG.2015.213