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127 related items for PubMed ID: 15998549

  • 1. No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population.
    Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Kato C, Ishijima M, Watanabe K, Kasai K, Kato N, Sasaki T.
    Neurosci Res; 2005 Sep; 53(1):91-4. PubMed ID: 15998549
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  • 3. Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.
    Li H, Yamagata T, Mori M, Momoi MY.
    Brain Dev; 2005 Apr; 27(3):207-10. PubMed ID: 15737702
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  • 9. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
    Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.
    Neurosci Lett; 2008 Aug 15; 441(1):56-60. PubMed ID: 18597938
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  • 12. Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population.
    Park Y, Won S, Nam M, Chung JH, Kwack K.
    J Child Neurol; 2014 Dec 15; 29(12):NP207-11. PubMed ID: 24356376
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  • 19. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.
    Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, Asaka T, Liu HX, Jin D, Koizumi K, Islam MS, Huang JJ, Ma WJ, Kim UH, Kim SJ, Park K, Kim D, Kikuchi M, Ono Y, Nakatani H, Suda S, Miyachi T, Hirai H, Salmina A, Pichugina YA, Soumarokov AA, Takei N, Mori N, Tsujii M, Sugiyama T, Yagi K, Yamagishi M, Sasaki T, Yamasue H, Kato N, Hashimoto R, Taniike M, Hayashi Y, Hamada J, Suzuki S, Ooi A, Noda M, Kamiyama Y, Kido MA, Lopatina O, Hashii M, Amina S, Malavasi F, Huang EJ, Zhang J, Shimizu N, Yoshikawa T, Matsushima A, Minabe Y, Higashida H.
    Neurosci Res; 2010 Jun 15; 67(2):181-91. PubMed ID: 20435366
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