© 1994 Oxford University Press
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Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p
Unité de Génétique Moléculaire Humaine, CNRS URA1445, Institut Pasteur 25 rue du Docteur Roux, 75724 Paris Cedex 15
1INSERM U134 H
pital de la Salp
trière 47 Bd de I'H
pital, 75013 Paris, France
2Fédération de Neurologie, H
pital de la Salptrière 47 Bd de I'H
pital, 75013 Paris, France
3Department of Neurology, Oudennjn Hospital Utrecht Netherlands
4Service de Neurologie, Centre Raymond Garcin, H
pital Ste-Anne 1 rue Cabanis, 75674 Paris Cedex 14, France
5MGC-Department of Human Genetics, Leiden University Leiden Netherlands
6INSERM U298, H
pital de la Salp
trière 47 Bd de l'H
pital, 75013 Paris
7INSERM U360, H
pital de la Salp
trière 47 Bd de l'H
pital, 75013 Paris
8INSERM U393, H
pital Necker 149 rue de Sèvres, 75743 Paris Cedex 15, France
9Department of Neurology, Nijmegen University Nijmegen, Netherlands
* To whom correspondence should be addressed
Received April 13, 1994; Revised June 29, 1994; Accepted June 29, 1994
Autosomal dominant familial spastic paraplegia (ADFSP) is a genetically heterogeneous neurodegenerative disorder characterized by a spasticity of the lower limbs. A locus causing AD-FSP (FSP1) has been previously mapped to chromosome 14q. We now report linkage of a second AD-FSP locus (FSP2) to chromosome 2p21 p24 In five of seven French families and one large Dutch pedigree. The analysis of recombination events and multipoint linkage place FSP2 within a 4 cM interval flanked by loci D2S400 and D2S367.
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