(RIKEN) Researchers from the Global Research Cluster in Japan have developed a potential mouse model for the genetic disorder known as an NGLY1 deficiency. Published in the journal PLOS Genetics, the study describes how a second knockout produces mice that survive after birth and have symptoms that are analogous to humans with NGLY1-deficiency.
from EurekAlert! - Social and Behavioral Science http://ift.tt/2oZR5AJ
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