A Locus Identified on Chromosome18P11.31 is Associated with Hippocampal Abnormalities in a Family with Mesial Temporal Lobe Epilepsy

We aimed to identify the region harboring a putative candidate gene associated with hippocampal abnormalities (HAb) in a family with mesial temporal lobe epilepsy (MTLE). Genome-wide scan was performed in one large kindred with MTLE using a total of 332 microsatellite markers at ∼12 cM intervals. An...

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Hlavní autoři: Maurer-Morelli, Cláudia V., Secolin, Rodrigo, Morita, Márcia E., Domingues, Romênia R., Marchesini, Rafael B., Santos, Neide F., Kobayashi, Eliane, Cendes, Fernando, Lopes-Cendes, Iscia
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Research Foundation 2012
Témata:
Neuroscience
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3449496/
https://ncbi.nlm.nih.gov/pubmed/23015801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2012.00124
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