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European Journal of Paediatric Neurology
Volumn 6, Issue SUPPL. 1, 2002, Pages
The genetics of Aicardi-Goutières syndrome
Author keywords

[No Author keywords available]
Indexed keywords

AICARDI GOUTIERES SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOMAL LOCALIZATION; CONSANGUINITY; DNA SEQUENCE; GENE LOCATION; GENE LOCUS; GENETIC ANALYSIS; GENOME ANALYSIS; HUMAN; MEIOSIS; MOLECULAR CLONING; PRIORITY JOURNAL; RISK ASSESSMENT; SEQUENCE ANALYSIS;
EID: 10944222190     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1053/ejpn.2002.0571     Document Type: Article
Times cited : (6)
References (4)
  • 1
    • 0021336060 scopus 로고
    • A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis
    • Aicardi J, Goutières F. A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis. Ann Neurol 1984; 15: 49-54.
    • (1984) Ann Neurol , vol.15 , pp. 49-54
    • Aicardi, J.1    Goutières, F.2
  • 2
    • 0033625515 scopus 로고    scopus 로고
    • AicardiGoutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21
    • Crow YJ, Jackson AP, Roberts E et al. AicardiGoutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21. Am J Hum Genet 2000; 67: 213-221.
    • (2000) Am J Hum Genet , vol.67 , pp. 213-221
    • Crow, Y.J.1    Jackson, A.P.2    Roberts, E.3
  • 3
    • 0032589399 scopus 로고    scopus 로고
    • Aicardi-Goutières syndrome: Monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?
    • Fauré S, Bordelais I, Marquette C et al. Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease? Clin Genet 1999; 56: 149-153.
    • (1999) Clin Genet , vol.56 , pp. 149-153
    • Fauré, S.1    Bordelais, I.2    Marquette, C.3
  • 4
    • 0032869123 scopus 로고    scopus 로고
    • Molecular genetics of the Finnish disease heritage
    • Peltonen L, Jalanko J, Varilo T. Molecular genetics of the Finnish disease heritage. Hum Mol Genet 1999; 8: 1913-1923.
    • (1999) Hum Mol Genet , vol.8 , pp. 1913-1923
    • Peltonen, L.1    Jalanko, J.2    Varilo, T.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.