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Dynamin 2 Mutations Cause Sporadic Centronuclear Myopathy with Neonatal Onset
(Wiley-Liss, 2007-12)
Neuropathologic Heterogeneity in HDDD1: A Familial Frontotemporal Lobar Degeneration With Ubiquitin-positive Inclusions and Progranulin Mutation
(Lippincott Williams & Wilkins, 2007-03)