Carosi, L., Giudice, T., Lullo, M., Lombardi, F., Babalini, C., Gaudiello, F., et al. (2015). Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10. JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY, 86(6), 702-704 [10.1136/jnnp-2014-308625].

Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10

CAROSI, LAURA;GAUDIELLO, FABRIZIO;MASSA, ROBERTO;ORLACCHIO, ANTONIO
2015-01-01

2015
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/26 - NEUROLOGIA
English
Con Impact Factor ISI
GENETICS; HEREDIT SPASTIC PARAPLEGIA; NEUROGENETICS; Adult; Age of Onset; Aged; Cognition Disorders; Disability Evaluation; Disease Progression; Female; Humans; Kinesin; Male; Middle Aged; Mutation; Phenotype; Spastic Paraplegia, Hereditary; Young Adult; Neurology (clinical); Psychiatry and Mental Health; Surgery; Arts and Humanities (miscellaneous); Medicine (all)
http://jnnp.bmj.com/content/86/6/702.full.pdf+html
Carosi, L., Giudice, T., Lullo, M., Lombardi, F., Babalini, C., Gaudiello, F., et al. (2015). Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10. JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY, 86(6), 702-704 [10.1136/jnnp-2014-308625].
Carosi, L; Giudice, T; Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, G; Massa, R; Kawarai, T; Orlacchio, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/159280
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