Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jacques Puymirat"'
Autor:
Annie Levert, Patrick A. Dion, Cynthia Soderblom, Craig Blackstone, Guy A. Rouleau, Nicolas Dupré, Inge A. Meijer, Peng-Peng Zhu, Sandra Laurent, Michel Sylvain, Jacques Puymirat, Bernard Brais, Julia Stadler
Publikováno v:
Annals of Neurology. 61:599-603
Hereditary spastic paraplegias (HSPs) are characterized by progressive lower limb spasticity and weakness. Mutations in the SPG3A gene, which encodes the large guanosine triphosphatase atlastin, are the second most common cause of autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc30b1f64c9d6508b94ca4d47a3b0475
https://doi.org/10.1002/ana.21114
https://doi.org/10.1002/ana.21114
Autor:
Inge A, Meijer, Patrick, Dion, Sandra, Laurent, Nicolas, Dupré, Bernard, Brais, Annie, Levert, Jacques, Puymirat, Marie France, Rioux, Michel, Sylvain, Peng-Peng, Zhu, Cynthia, Soderblom, Julia, Stadler, Craig, Blackstone, Guy A, Rouleau
Publikováno v:
Annals of neurology. 61(6)
Hereditary spastic paraplegias (HSPs) are characterized by progressive lower limb spasticity and weakness. Mutations in the SPG3A gene, which encodes the large guanosine triphosphatase atlastin, are the second most common cause of autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::689e383cfe985a50c7bb0d39ef3847dc
https://pubmed.ncbi.nlm.nih.gov/17427918
https://pubmed.ncbi.nlm.nih.gov/17427918