Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum

Journal article

Peer reviewed

A Magariello, L Citrigno, S Zuchner, M Gonzalez, A Patitucci, V Sofia, F. L Conforti, I Pappalardo, R Mazzei, C Ungaro, …

European journal of neurology, Vol.21(3), pp.e25-e26

2014-03

PMID: 24517879

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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

Title: Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum
Creators: A Magariello - National Research Council
L Citrigno - National Research Council
S Zuchner - University of Miami
M Gonzalez - University of Miami
A Patitucci - National Research Council
V Sofia - Università di Catania
F. L Conforti - National Research Council
I Pappalardo - Università di Catania
R Mazzei - National Research Council
C Ungaro - National Research Council
M Zappia - Università di Catania
M Muglia - National Research Council
Publication Details: European journal of neurology, Vol.21(3), pp.e25-e26
Number of pages: 2
Academic Unit: Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Pediatrics - Mailman Center for Child Development
Language: English
Resource Type: Journal article
PMID: 24517879
Record Identifier: 991031562257302976