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المؤلفون: MUGLIA M, MAGARIELLO A, NICOLETTI, Giovanni Francesco, PATINUCCI A, GABIELE AL, CONFORTI FL, MAZZEI R, CARACCIOLO M, ARDITO B, LA STILLA M, QUATTRONE A., TEDESCHI, Gioacchino
المساهمون: Muglia, M, Magariello, A, Nicoletti, Giovanni Francesco, Patinucci, A, Gabiele, Al, Conforti, Fl, Mazzei, R, Caracciolo, M, Ardito, B, LA STILLA, M, Tedeschi, Gioacchino, Quattrone, A.
المصدر: Annals of neurology 51 (2002): 794–795.
info:cnr-pdr/source/autori:Muglia M,1; Magariello A,1; Nicoletti G,1; Patitucci A,1; Gabriele AL,1; Conforti FL,1; Mazzei R,1; Caracciolo M,1; Ardito B,2; Lastilla M,2; Tedeschi G,3; Quattrone A.1-4/titolo:Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia/doi:/rivista:Annals of neurology/anno:2002/pagina_da:794/pagina_a:795/intervallo_pagine:794–795/volume:51مصطلحات موضوعية: AD-HSP, atlastin, SPG3A gene, linkage, LOD score
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::82f35ddbddc6b2817d0523f6b9502fe3
https://publications.cnr.it/doc/49893