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Volumn 4, Issue 4, 2011, Pages 293-296

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set

Author keywords

Androgen receptor; Behavioral analysis of animal models; Developmental neurobiology; Sex differences; Testosterone

Indexed keywords

INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN;

EID: 80052721426     PISSN: 19393792     EISSN: 19393806     Source Type: Journal    
DOI: 10.1002/aur.195     Document Type: Article
Times cited : (2)

References (10)
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  • 2
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    • Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism
    • ics
    • Bhat, S.S., Ladd, S., Grass, F., Spence, J.E., Brasington, C.K., et al. (2008). Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism. Clinical Genetics, 73, 94-96.
    • (2008) Clinical Genet , vol.73 , pp. 94-96
    • Bhat, S.S.1    Ladd, S.2    Grass, F.3    Spence, J.E.4    Brasington, C.K.5
  • 4
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    • The autism genetic resource exchange: A resource for the study of autism and related neuropsychiatric conditions
    • Geschwind, D.H., Sowinski, J., Lord, C., Iversen, P., Shestack, J., et al. (2001). The autism genetic resource exchange: A resource for the study of autism and related neuropsychiatric conditions. American Journal of Human Genetics, 69, 463-466.
    • (2001) American Journal of Human Genetics , vol.69 , pp. 463-466
    • Geschwind, D.H.1    Sowinski, J.2    Lord, C.3    Iversen, P.4    Shestack, J.5
  • 5
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    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander, E., & Kruglyak, L. (1995). Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nature Genetics, 11, 241-247.
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    • Lander, E.1    Kruglyak, L.2
  • 6
    • 57049170205 scopus 로고    scopus 로고
    • Mutations in the calcium-related gene IL1RAPL1 are associated with autism
    • Piton, A., Michaud, J.L., Peng, H., Aradhya, S., Gauthier, J., et al. (2008). Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Human Molecular Genetics, 17, 3965-3974.
    • (2008) Human Molecular Genetics , vol.17 , pp. 3965-3974
    • Piton, A.1    Michaud, J.L.2    Peng, H.3    Aradhya, S.4    Gauthier, J.5
  • 7
    • 0001665187 scopus 로고    scopus 로고
    • Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
    • ics
    • Stromme, P., Mangelsdorf, M.E., Shaw, M.A., Lower, K.M., Lewis, S.M., et al. (2002). Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy. Nature Genetics, 30, 441-445.
    • (2002) Nature Genet , vol.30 , pp. 441-445
    • Stromme, P.1    Mangelsdorf, M.E.2    Shaw, M.A.3    Lower, K.M.4    Lewis, S.M.5
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    • Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation
    • Turner, G., Partington, M., Kerr, B., Mangelsdorf, M., & Gecz, J. (2002). Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation. American Journal of Medical Genetics, 112, 405-411.
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    • Turner, G.1    Partington, M.2    Kerr, B.3    Mangelsdorf, M.4    Gecz, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.