The family of genes implicated in hereditary spastic paraplegias (HSPs) is quickly expanding, mostly owing to the widespread availability of next-generation DNA sequencing methods. Nevertheless, a genetic diagnosis remains unavailable for many patients.

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia / Rinaldi, Carlo; Schmidt, Thomas; Situ, Alan J; Johnson, Janel O; Lee, Philip R; Chen, Ke Lian; Bott, Laura C; Fadó, Rut; Harmison, George H; Parodi, Sara; Grunseich, Christopher; Renvoisé, Benoît; Biesecker, Leslie G; DE MICHELE, Giuseppe; Santorelli, Filippo M; Filla, Alessandro; Stevanin, Giovanni; Dürr, Alexandra; Brice, Alexis; Casals, Núria; Traynor, Bryan J; Blackstone, Craig; Ulmer, Tobias S; Fischbeck, Kenneth H.. - In: JAMA NEUROLOGY. - ISSN 2168-6149. - 72:5(2015), p. 561-70. [10.1001/jamaneurol.2014.4769]

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia

DE MICHELE, GIUSEPPE;FILLA, ALESSANDRO;
2015

Abstract

The family of genes implicated in hereditary spastic paraplegias (HSPs) is quickly expanding, mostly owing to the widespread availability of next-generation DNA sequencing methods. Nevertheless, a genetic diagnosis remains unavailable for many patients.
2015
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia / Rinaldi, Carlo; Schmidt, Thomas; Situ, Alan J; Johnson, Janel O; Lee, Philip R; Chen, Ke Lian; Bott, Laura C; Fadó, Rut; Harmison, George H; Parodi, Sara; Grunseich, Christopher; Renvoisé, Benoît; Biesecker, Leslie G; DE MICHELE, Giuseppe; Santorelli, Filippo M; Filla, Alessandro; Stevanin, Giovanni; Dürr, Alexandra; Brice, Alexis; Casals, Núria; Traynor, Bryan J; Blackstone, Craig; Ulmer, Tobias S; Fischbeck, Kenneth H.. - In: JAMA NEUROLOGY. - ISSN 2168-6149. - 72:5(2015), p. 561-70. [10.1001/jamaneurol.2014.4769]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/614040
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