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Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene

✍ Scribed by Alías, L.; Barceló, M.J.; Bernal, S.; Martínez-Hernández, R.; Also-Rallo, E.; Vázquez, C.; Santana, A.; Millán, J.M.; Baiget, M.; Tizzano, E.F.

Book ID: 120591825
Publisher: John Wiley and Sons
Year: 2013
Tongue: English
Weight: 649 KB
Volume: 85
Category: Article
ISSN: 0009-9163
DOI: 10.1111/cge.12222

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