Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

Autor Züchner, Stephan, Wang, Gaofeng, Tran-Viet, Khanh-Nhat, Nance, Martha A., Gaskell, Perry C., Vance, Jeffery M., Ashley-Koch, Allison E., Pericak-Vance, Margaret A.
Vydáno 2006

A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

Autor Reid, Evan, Kloos, Mark, Ashley-Koch, Allison, Hughes, Lori, Bevan, Simon, Svenson, Ingrid K., Graham, Felicia Lennon, Gaskell, Perry C., Dearlove, Andrew, Pericak-Vance, Margaret A., Rubinsztein, David C., Marchuk, Douglas A.
Vydáno 2002

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers

Autor Schellenberg, Gerard D., Pericak-Vance, Margaret A., Wijsman, Ellen M., Moore, Deborah K., Gaskell, Perry C., Yamaoka, Larry A., Bebout, Jacqueline L., Anderson, Leojean, Welsh, Kathleen A., Clark, Christopher M., Martin, George M., Roses, Allen D., Bird, Thomas D.
Vydáno 1991

A genome-wide linkage analysis of dementia in the Amish

Autor Hahs, Daniel W., McCauley, Jacob L., Crunk, Amy E., McFarland, Lynne L., Gaskell, Perry C., Jiang, Lan, Slifer, Susan H., Vance, Jeffery M., Scott, William K., Welsh-Bohmer, Kathleen A., Johnson, Stephanie R., Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L.
Vydáno 2006