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W Sproviero

Showing results (1-10 of 4) with videos related to

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Human Genetics|February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancyF E Rocca, E V De Marco, F Annesi, et al.
Human Genetics|April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson diseaseP Tarantino, F Annesi, V Scornaienchi, et al.
BMC Bioinformatics|April 29, 2019
DNAscan: personal computer compatible NGS analysis, annotation and visualisationA Iacoangeli, A Al Khleifat, W Sproviero, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosisF L Conforti, W Sproviero, I L Simone, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Human Genetics|February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancyF E Rocca, E V De Marco, F Annesi, et al.
Human Genetics|April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson diseaseP Tarantino, F Annesi, V Scornaienchi, et al.
BMC Bioinformatics|April 29, 2019
DNAscan: personal computer compatible NGS analysis, annotation and visualisationA Iacoangeli, A Al Khleifat, W Sproviero, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosisF L Conforti, W Sproviero, I L Simone, et al.
Pageof 1