Department for Sustainability

Found 2 results

Filters: Author is Santoro, L. [Clear All Filters]

2005

Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations., Patrono, Clarice, Scarano V., Cricchi F., Melone M.A., Chiriaco M., Napolitano A., Malandrini A., De Michele G., Petrozzi L., Giraldi C., et al. , Human mutation, Volume 25, Number 5, p.506, (2005)

2000

A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency, Santoro, L., Carrozzo R., Malandrini A., Piemonte F., Patrono Clarice, Villanova M., Tessa A., Palmeri S., Bertini E., and Santorelli F.M. , Neuromuscular Disorders, Volume 10, Number 6, p.450-453, (2000)