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http://purl.uniprot.org/citations/15007136http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15007136http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15007136http://www.w3.org/2000/01/rdf-schema#comment"The authors describe clinical, neuroimaging and molecular findings in a group of 15 patients with classic lissencephaly (LIS) and subcortical band heterotopia (SBH). A 1385A-->C mutation was found in the LIS1 gene in one patient with LIS more severe than expected for individuals with missense mutations in LIS1. The authors believe that the site of the mutation, present in a functionally critical region of the protein, could explain the unusual severe phenotype found in this patient."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.org/dc/terms/identifier"doi:10.1212/01.wnl.0000113725.46254.fd"xsd:string
http://purl.uniprot.org/citations/15007136http://purl.org/dc/terms/identifier"doi:10.1212/01.wnl.0000113725.46254.fd"xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Lopes-Cendes I."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Lopes-Cendes I."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Marques-de-Faria A.P."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Marques-de-Faria A.P."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Cendes F."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Cendes F."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Guerreiro M.M."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Guerreiro M.M."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Montenegro M.A."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Montenegro M.A."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Torres F.R."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/author"Torres F.R."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/name"Neurology"xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/name"Neurology"xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/pages"799-802"xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/pages"799-802"xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/title"Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia."xsd:string
http://purl.uniprot.org/citations/15007136http://purl.uniprot.org/core/title"Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia."xsd:string