TY  - GEN
AU  - Klebe,Stephan
AU  - Lacour,Arnaud
AU  - Durr,Alexandra
AU  - Stojkovic,Tanya
AU  - Depienne,Christel
AU  - Forlani,Sylvie
AU  - Poea-Guyon,Sandrine
AU  - Vuillaume,Isabelle
AU  - Sablonniere,Bernard
AU  - Vermersch,Patrick
AU  - Brice,Alexis
AU  - Stevanin,Giovanni
TI  - NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe
SN  - 1364-6745
PY  - 2008///0123
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Amino Acid Substitution
KW  - Child
KW  - Europe
KW  - Exons
KW  - Female
KW  - Genes, Dominant
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - genetics
KW  - Mutation
KW  - Paraplegia
N1  - Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s10048-006-0074-9
ER  -