ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism

Bibliographic Details

Published in:	Brain (London, England : 1878) England : 1878), 2016-01, Vol.139 (Pt 1), p.e3-e3
Main Authors:	Panza, Emanuele, Escamilla-Honrubia, Juan M, Marco-Marín, Clara, Gougeard, Nadine, De Michele, Giuseppe, Morra, Vincenzo Brescia, Liguori, Rocco, Salviati, Leonardo, Donati, Maria Alice, Cusano, Roberto, Pippucci, Tommaso, Ravazzolo, Roberto, Németh, Andrea H, Smithson, Sarah, Davies, Sally, Hurst, Jane A, Bordo, Domenico, Rubio, Vicente, Seri, Marco
Format:	Article
Language:	eng
Subjects:	Aldehyde Dehydrogenase - genetics Female Humans Male Mutation - genetics Ornithine - genetics Ornithine - metabolism Spastic Paraplegia, Hereditary - genetics
Online Access:	Get full text
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