The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation

Lucia Ricciardi; Simona Petrucci; Daniela Di Giuda; Laura Serra; Barbara Spanò; Mariachiara Sensi; Monia Ginevrino; Fabrizio Cocciolillo; Marco Bozzali; Enza Maria Valente; Alfonso Fasano

doi:10.1002/mds.26549

The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation

Lucia Ricciardi, Simona Petrucci, Daniela Di Giuda, Laura Serra, Barbara Spanò, Mariachiara Sensi, Monia Ginevrino, Fabrizio Cocciolillo, Marco Bozzali, Enza Maria Valente, Alfonso Fasano

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	257-8
Number of pages	2
Journal	Movement Disorders
Volume	31
Issue number	2
DOIs	https://doi.org/10.1002/mds.26549
Publication status	Published - Feb 2016

Keywords

Adult
Female
Humans
Male
Middle Aged
Mutation
Parkinson Disease
Pedigree
Phenotype
alpha-Synuclein
Letter
Research Support, Non-U.S. Gov't

Access to Document

10.1002/mds.26549

Cite this

Ricciardi, L., Petrucci, S., Di Giuda, D., Serra, L., Spanò, B., Sensi, M., Ginevrino, M., Cocciolillo, F., Bozzali, M., Valente, E. M., & Fasano, A. (2016). The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation. Movement Disorders, 31(2), 257-8. https://doi.org/10.1002/mds.26549

The Contursi Family 20 Years Later : Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation. / Ricciardi, Lucia; Petrucci, Simona; Di Giuda, Daniela; Serra, Laura; Spanò, Barbara; Sensi, Mariachiara; Ginevrino, Monia; Cocciolillo, Fabrizio; Bozzali, Marco ; Valente, Enza Maria; Fasano, Alfonso.

In: Movement Disorders, Vol. 31, No. 2, 02.2016, p. 257-8.

Research output: Contribution to journal › Article

Ricciardi, Lucia ; Petrucci, Simona ; Di Giuda, Daniela ; Serra, Laura ; Spanò, Barbara ; Sensi, Mariachiara ; Ginevrino, Monia ; Cocciolillo, Fabrizio ; Bozzali, Marco ; Valente, Enza Maria ; Fasano, Alfonso. / The Contursi Family 20 Years Later : Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation. In: Movement Disorders. 2016 ; Vol. 31, No. 2. pp. 257-8.

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