Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
Fonknechten N; Mavel D; Byrne P; Davoine CS; Cruaud C; Bönsch D; Samson D; Coutinho P; Hutchinson M; McMonagle P; Burgunder JM; Tartaglione A; Heinzlef O; Feki I; Deufel T; Parfrey N; Brice A; Fontaine B; Prud'homme JF; Weissenbach J; Dürr A; Hazan J; Human Molecular Genetics, 2000, vol. 9, issue 4, p 637, ISSN 09646906. ISBN 09646906.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef