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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2008-3-11
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pubmed:abstractText |
To perform a clinical and genetic study of Tunisian families with autosomal recessive (AR) hereditary spastic paraplegia with thin corpus callosum (HSP-TCC).
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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 |
Mar
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pubmed:issn |
0003-9942
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pubmed:author |
pubmed-author:BelalSamirS,
pubmed-author:BoukhrisAmirA,
pubmed-author:BriceAlexisA,
pubmed-author:DenisElodieE,
pubmed-author:DenoraPaolaP,
pubmed-author:ElleuchNizarN,
pubmed-author:FekiImedI,
pubmed-author:MhiriChokriC,
pubmed-author:MiladiMohamed ImedMI,
pubmed-author:StevaninGiovanniG,
pubmed-author:TruchettoJérémyJ
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pubmed:issnType |
Print
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
393-402
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:18332254-Adult,
pubmed-meshheading:18332254-Agenesis of Corpus Callosum,
pubmed-meshheading:18332254-DNA Mutational Analysis,
pubmed-meshheading:18332254-Family Health,
pubmed-meshheading:18332254-Female,
pubmed-meshheading:18332254-Genetic Heterogeneity,
pubmed-meshheading:18332254-Genotype,
pubmed-meshheading:18332254-Humans,
pubmed-meshheading:18332254-Magnetic Resonance Imaging,
pubmed-meshheading:18332254-Male,
pubmed-meshheading:18332254-Mental Disorders,
pubmed-meshheading:18332254-Phenotype,
pubmed-meshheading:18332254-Proteins,
pubmed-meshheading:18332254-Spastic Paraplegia, Hereditary,
pubmed-meshheading:18332254-Tunisia
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pubmed:year |
2008
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pubmed:articleTitle |
Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
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pubmed:affiliation |
Department of Neurology, Habib Bourguiba University Hospital, Tunis, Tunisia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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