C3orf58

C3orf58

C3orf58 is a human gene. It was highlighted in a screen for genes possibly related to autism. The authors propose that the gene should be renamed Deleted in autism-1 (DIA1). Experiments in a rat neuronal cell culture model suggested that this gene may be regulated directly or indirectly by MEF2 site binding proteins. [cite journal | author=Morrow EM, Yoo SY, Flavell SW, "et al." |title=Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry. |journal=Science |volume=321 |issue= 5886 |pages= 218-223 |year= 2008 |pmid= |doi= 10.1126/science.1157657 ]

ee also

* Heritability of autism

References


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  • Heritability of autism — Autism has a strong genetic basis, although the genetics of autism is complex and it is unclear whether ASD is explained more by multigene interactions or by rare mutations with major effects. [cite journal |journal= Nat Rev Genet |year=2008… …   Wikipedia

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