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Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments
Journal article   Peer reviewed

Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments

A Magariello, C Russo, L Citrigno, S Züchner, A Patitucci, R Mazzei, F.L Conforti, E Ferlazzo, U Aguglia and M Muglia
Journal of the neurological sciences, Vol.372, pp.347-349
2017-01-15
PMID: 28017243

Abstract

SPG35 Hereditary Spastic Paraplegia FA2H gene Exome sequencing

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Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.52 Neurodegenerative Diseases
1.52.951 Huntington's Disease
Web Of Science research areas
Clinical Neurology
Neurosciences
ESI research areas
Neuroscience & Behavior

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#3 Good Health and Well-Being

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