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Association of common variants in the Joubert syndrome gene (AHI1) with autism
It has been suggested that autism, like other complex genetic disorders, may benefit from the study of rare or Mendelian variants associated with syndromic or non-syndromic forms of the disease. However, there are few examples in which common variation in genes causing a Mendelian neuropsychiatric d...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2638573/ https://ncbi.nlm.nih.gov/pubmed/18782849 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn291 |
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