De novo mutations in SPG3A: a challenge in differential diagnosis and genetic counselling

Luca Leonardi; Christian Marcotulli; Filippo M. Santorelli; Alessandra Tessa; Carlo Casali

doi:10.1007/s10072-015-2097-1

De novo mutations in SPG3A: a challenge in differential diagnosis and genetic counselling

Luca Leonardi, Christian Marcotulli, Filippo M. Santorelli, Alessandra Tessa, Carlo Casali

Fondazione Stella Maris

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	1063-1064
Number of pages	2
Journal	Neurological Sciences
Volume	36
Issue number	6
DOIs	https://doi.org/10.1007/s10072-015-2097-1
Publication status	Published - Jun 5 2015

ASJC Scopus subject areas

Clinical Neurology
Psychiatry and Mental health
Dermatology

Access to Document

10.1007/s10072-015-2097-1

Cite this

Leonardi, L., Marcotulli, C., Santorelli, F. M., Tessa, A., & Casali, C. (2015). De novo mutations in SPG3A: a challenge in differential diagnosis and genetic counselling. Neurological Sciences, 36(6), 1063-1064. https://doi.org/10.1007/s10072-015-2097-1

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