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Volumn 78, Issue 17, 2012, Pages 1299-1303

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT LATERAL TEMPORAL EPILEPSY; CLINICAL ARTICLE; COPY NUMBER VARIATION; FAMILY STUDY; FEMALE; FOCAL EPILEPSY; GENE; GENE DELETION; GENE DOSAGE; GENOTYPE; HUMAN; LGI1 GENE; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TEMPORAL LOBE EPILEPSY;

EID: 84860745441     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3182518328     Document Type: Article
Times cited : (28)

References (10)
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  • 3
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    • Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
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  • 5
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    • LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy
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    • (2009) Hum Mutat , vol.30 , pp. 530-536
    • Nobile, C.1    Michelucci, R.2    Andreazza, S.3
  • 6
    • 77956308262 scopus 로고    scopus 로고
    • Evaluation of depression risk in LGI1 mutation carriers
    • Heiman GA, Kamberakis K, Gill R, et al. Evaluation of depression risk in LGI1 mutation carriers. Epilepsia 2010; 51:1685-1690.
    • (2010) Epilepsia , vol.51 , pp. 1685-1690
    • Heiman, G.A.1    Kamberakis, K.2    Gill, R.3
  • 7
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    • PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • DOI 10.1101/gr.6861907
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  • 9
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    • 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
    • Helbig I, Mefford HC, Sharp AJ, et al. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat Genet 2009;41:160-162.
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  • 10
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    • DOI 10.1038/ng1090
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.