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Mutation in CPT1C associated with pure autosomal dominant spastic paraplegia
Carlo Rinaldi*, Thomas Schmidt, Alan J. Situ, Janel O. Johnson, Philip R. Lee, Ke Lian Chen, Laura C. Bott, Rut Fadó, George H. Harmison, Sara Parodi, Christopher Grunseich, Benoît Renvoisé, Leslie G. Biesecker, Giuseppe De Michele, Filippo M. Santorelli, Alessandro Filla, Giovanni Stevanin, Alexandra Dürr, Alexis Brice, Núria Casals
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
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