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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
14
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pubmed:dateCreated |
2009-10-6
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pubmed:abstractText |
Hereditary spastic paraplegias (HSPs) are very heterogeneous inherited neurodegenerative disorders. Our group recently identified ZFYVE26 as the gene responsible for one of the clinical and genetic entities, SPG15. Our aim was to describe its clinical and mutational spectra.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1526-632X
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pubmed:author |
pubmed-author:Auer-GrumbachMM,
pubmed-author:BoukhrisAA,
pubmed-author:BriceAA,
pubmed-author:CoutinhoPP,
pubmed-author:DurrAA,
pubmed-author:FernandezJ CJC,
pubmed-author:ForlaniSS,
pubmed-author:GoderGG,
pubmed-author:GoizetCC,
pubmed-author:Guyant-MaréchalLL,
pubmed-author:HaneinSS,
pubmed-author:JonveauxPP,
pubmed-author:LoureiroJJ,
pubmed-author:MalteteDD,
pubmed-author:Martin-HardyPP,
pubmed-author:MelkaRR,
pubmed-author:MhiriCC,
pubmed-author:MundwillerEE,
pubmed-author:OrignacII,
pubmed-author:RoelensFF,
pubmed-author:SibonII,
pubmed-author:SolaCC,
pubmed-author:StevaninGG,
pubmed-author:TruchettoJJ
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pubmed:issnType |
Electronic
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pubmed:day |
6
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1111-9
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pubmed:meshHeading |
pubmed-meshheading:19805727-Adolescent,
pubmed-meshheading:19805727-Brain,
pubmed-meshheading:19805727-Carrier Proteins,
pubmed-meshheading:19805727-Child,
pubmed-meshheading:19805727-Corpus Callosum,
pubmed-meshheading:19805727-Female,
pubmed-meshheading:19805727-Humans,
pubmed-meshheading:19805727-Magnetic Resonance Imaging,
pubmed-meshheading:19805727-Male,
pubmed-meshheading:19805727-Mutation,
pubmed-meshheading:19805727-Positron-Emission Tomography,
pubmed-meshheading:19805727-Severity of Illness Index,
pubmed-meshheading:19805727-Spastic Paraplegia, Hereditary,
pubmed-meshheading:19805727-Tomography, Emission-Computed, Single-Photon
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pubmed:year |
2009
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pubmed:articleTitle |
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.
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pubmed:affiliation |
INSERM, U975, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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