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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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| Publicado en: | Am J Med Genet B Neuropsychiatr Genet |
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| Autores principales: | , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Wiley-Blackwell
2003
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| Materias: | |
| Acceso en línea: | 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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