Persistent URL of this record https://hdl.handle.net/1887/122225
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Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A
- All authors
- Tao, F.F.; Beecham, G.W.; Rebelo, A.P.; Svaren, J.; Blanton, S.H.; Moran, J.J.; Lopez-Anido, C.; Morrow, J.M.; Abreu, L.; Rizzo, D.; Kirk, C.A.; Wu, X.Y.; Feely, S.; Verhamme, C.; Saporta, M.A.; Herrmann, D.N.; Day, J.W.; Sumner, C.J.; Lloyd, T.E.; Li, J.; Yum, S.W.; Taroni, F.; Baas, F.; Choi, B.O.; Pareyson, D.; Scherer, S.S.; Reilly, M.M.; Shy, M.E.; Zuchner, S.; Lewis, R.; Acsadi, G.; Finkel, R.; Fridman, V.; Ramchandren, S.; Walk, D.; Logigian, E.; Stanton, M.; Eichinger, K.; Guntrum, D.; Gibson, C.; Burns, J.; Moroni, I.; Pisciotta, C.; Laura, M.; Muntoni, F.; Sowden, J.E.; Mountain, J.; Bai, Y.H.; Bacon, C.; Gutmann, L.; Grider, T.; Phetteplace, J.; Seyedsadjadi, R.; Houlden, H.; Cortese, A.; Pandraud, A.; Calabrese, D.; Saveri, P.; Richardson, J.; Dankwa, L.; Lee, D.; Siskind, C.; Maciel, R.; Bis, D.; Inherited Neuropathy Consortium
- Date
- 2019-03-01
- Journal
- Annals of Neurology
- Volume
- 85
- Issue
- 3
- Pages
- 316 - 330