Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
Nature Genetics1999Vol. 23(3), pp. 296–303
Citations Over TimeTop 10% of 1999 papers
Jamïlé Hazan, Núria Fonknechten, Delphine Mavel, Caroline Paternotte, Delphine Samson, François Artiguenave, Claire-Sophie Davoine, Corinne Cruaud, Alexandra Dürr, Patrick Wincker, Philippe Brottier, Laurence Cattolico, Valérie Barbe, Jean‐Marc Burgunder, Jean-François Prud'homme, Alexis Brice, Bertrand Fontaine, Roland Heilig, Jean Weissenbach
Related Papers
- → Clinical and genetic heterogeneity in hereditary spastic paraplegias: From SPG1 to SPG72 and still counting(2015)181 cited
- → Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families(2021)14 cited
- → A novel homozygous mutation in ATP13A2 gene causing pure hereditary spastic paraplegia(2021)3 cited
- → phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia(2019)
- → 788: HOMOZYGOUS NONSENSE MUTATION IN ARL6IP1 LEADS TO SEVERE PHENOTYPE OF HEREDITARY SPASTIC PARAPLEGIA(2021)