Biochemical studies shed light on disease mechanism
Author: Editor
Mitochondrial dysfunction in HSPs & Ataxias
Disease-causing mechanisms described
New light shed on SPG78 mechanism
Multi-faceted studies the key
Function of PCYT2 gene (SPG82) studied
Key enzyme in muscle health and degeneration
New HSP genotypes & phenotypes
Research from Iran, Germany, Canada, Sweden, Sudan, France, China, South Korea, India
Vale Alan Mackay-Sim
Outstanding scientist & dear friend of the HSP community
Rare Disease Day, 28 February
Celebrate Rare Disease Day to raise public awareness
Adelaide Open Garden event, 11 – 13 March
Fundraiser for HSP research
Recent Social Events
Adelaide, Hobart, Melbourne
SP Foundation (US) research funding awards
Over $1 million goes to 7 projects