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Autor:
Jamilé Hazan, Judith C.T. van Deutekom, George W. Padberg, Jean Welssenbach, Yves Agid, Catherine Lamy, Judith Melkl, Arnold Munnich, Richard P. M. Bruyn, Bertrand Fontaine, Olivier Lyon-Caen, Rune R. Frants, Alexandra Durr, Clalre-Sophie Rime, Alexis Brice, Jean de Recondo
Publikováno v:
Human molecular genetics. 3(9)
Autosomal dominant familial spastic paraplegia (AD-FSP) 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 rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13c8cf20d3b61058855bd96f8a61b94f
https://pubmed.ncbi.nlm.nih.gov/7833913
https://pubmed.ncbi.nlm.nih.gov/7833913
