A Mutation that Lowers Risk for Schizophrenia?
Last month, Rees et al. (2014) reported that, in contrast to copy number variant (CNV) deletions at the genetic locus, 22q11, which increase schizophrenia risk, duplications in that same region […]
Last month, Rees et al. (2014) reported that, in contrast to copy number variant (CNV) deletions at the genetic locus, 22q11, which increase schizophrenia risk, duplications in that same region […]
“How a genotype and its environment interact to yield a phenotype poses a vast epistemological gap. Proteins that exhibit conformational diversity and contingent functional multiplicity increase the dimensions of phenotypic […]
In a study published this month in the journal, Science, Tyzio et al. (2014) report some exciting findings which help fill in some of the gaps on oxytocin research in […]
I’ve talked about Fragile X Syndrome before and its relationship to autism, albeit briefly. What I didn’t touch on, however, is that Fragile X Syndrome (FXS) isn’t the only condition […]
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