- Title
- Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments
- Creators
- A Magariello - Institute of Neurological Sciences, National Research Council, Mangone, CS, ItalyC Russo - Regional Epilepsy Centre, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, ItalyL Citrigno - Institute of Neurological Sciences, National Research Council, Mangone, CS, ItalyS Züchner - Department of Human Genetics and Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL 33136, USAA Patitucci - Institute of Neurological Sciences, National Research Council, Mangone, CS, ItalyR Mazzei - Institute of Neurological Sciences, National Research Council, Mangone, CS, ItalyF.L Conforti - Institute of Neurological Sciences, National Research Council, Mangone, CS, ItalyE Ferlazzo - Regional Epilepsy Centre, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, ItalyU Aguglia - Regional Epilepsy Centre, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, ItalyM Muglia - Institute of Neurological Sciences, National Research Council, Mangone, CS, Italy
- Publication Details
- Journal of the neurological sciences, Vol.372, pp.347-349
- Publisher
- Elsevier B.V
- Academic Unit
- Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics
- Language
- English
- Resource Type
- Journal article
- PMID
- 28017243
- Record Identifier
- 991031599220102976
Journal article
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments
Journal of the neurological sciences, Vol.372, pp.347-349
2017-01-15
PMID: 28017243
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- Collaboration types
- 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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Source: InCites