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A review of the evidence for the canonical Wnt pathway in autism spectrum disorders
Microdeletion and microduplication copy number variations are found in patients with autism spectrum disorder and in a number of cases they include genes that are involved in the canonical Wnt signaling pathway (for example, FZD9, BCL9 or CDH8). Association studies investigating WNT2, DISC1, MET, DO...
Uloženo v:
| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3492093/ https://ncbi.nlm.nih.gov/pubmed/23083465 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-3-10 |
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