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Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene in patients with autism

Infantile autism is a pervasive developmental disorder with a strong genetic component. The mode of inheritance appears to be complex and no specific susceptibility genes have yet been identified. Chromosome 16p13.3 may contain a susceptibility gene based on findings from genome scans and reports of...

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Detalhes bibliográficos
Publicado no:Am J Med Genet B Neuropsychiatr Genet
Main Authors: Lauritsen, Marlene, Nyegaard, Mette, Betancur, Catalina, Colineaux, Catherine, Josiassen, Trine, Kruse, Torben, Leboyer, Marion, Ewald, Henrik
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley-Blackwell 2003
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4830897/
https://ncbi.nlm.nih.gov/pubmed/12898583
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.20050
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