Spastic paraplegia 13, autosomal dominant (medical condition)

A rare genetic disorder characterized mainly by progressive spasticity and weakness of the lower legs. See also Spastic paraplegia 13, autosomal dominant

Chemwatch
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.