Search by property

This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• Bouwkamp 2018 Neurol Genet  + (Bouwkamp CG, Afawi Z, Fattal-Valevski A, K … Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA (2018) ''ACO2'' homozygous missense mutation associated with complicated hereditary spastic paraplegia. Neurol Genet 4:e223.y spastic paraplegia. Neurol Genet 4:e223.)

• Bouwkamp 2018 Neurol Genet  +