| pubmed-article:11914408 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11914408 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:11914408 | lifeskim:mentions | umls-concept:C0205108 | lld:lifeskim |
| pubmed-article:11914408 | lifeskim:mentions | umls-concept:C2678104 | lld:lifeskim |
| pubmed-article:11914408 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:11914408 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:11914408 | lifeskim:mentions | umls-concept:C1414635 | lld:lifeskim |
| pubmed-article:11914408 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:11914408 | pubmed:dateCreated | 2002-3-26 | lld:pubmed |
| pubmed-article:11914408 | pubmed:abstractText | To examine the clinical and MRI associations in bilateral periventricular nodular heterotopia (BPNH) (MIM # 300049) in two families segregating a missense mutation and a C-terminal deletion of the filamin 1(FLN1) gene. | lld:pubmed |
| pubmed-article:11914408 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11914408 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11914408 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:11914408 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11914408 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:11914408 | pubmed:issn | 0028-3878 | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:GuerriniRR | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:MoraHH | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:TonioloDD | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:CarrozzoRR | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:VeggiottiPP | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:TortorellaGG | lld:pubmed |
| pubmed-article:11914408 | pubmed:author | pubmed-author:VolzoneAA | lld:pubmed |
| pubmed-article:11914408 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11914408 | pubmed:day | 26 | lld:pubmed |
| pubmed-article:11914408 | pubmed:volume | 58 | lld:pubmed |
| pubmed-article:11914408 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11914408 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11914408 | pubmed:pagination | 916-21 | lld:pubmed |
| pubmed-article:11914408 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:11914408 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:11914408 | pubmed:articleTitle | Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. | lld:pubmed |
| pubmed-article:11914408 | pubmed:affiliation | Neurogenetics Laboratory, Division of Child Neurology and Psychiatry, University of Pisa, Italy. | lld:pubmed |
| pubmed-article:11914408 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11914408 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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