Wilson disease: Genetic mutation
Wilson disease (copper storage disease) is a rare genetic disorder in which one or more genetic mutations disrupt copper metabolism
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Wilson disease (copper storage disease) is a rare genetic disorder in which one or more genetic mutations disrupt copper metabolism
Read moreThe genetic and genomic revolutions have led to an abundance of data about the genetic factors that confer a predisposition
Read moreGenetic testing improves the diagnoses of abnormalities in developing babies that are picked up during ultrasound scans, scientists report today
Read moreGenetic variants which prevent a neurotransmitter receptor from working properly have been implicated in the development of schizophrenia, according to
Read moreResearchers at the Icahn School of Medicine at Mount Sinai and The Rockefeller University have discovered a new use for
Read more(HealthDay)—Vitrakvi (larotrectinib) has been approved by the U.S. Food and Drug Administration to treat adult and pediatric patients whose cancers
Read moreBy combining data on individuals’ lifetime sun exposure and their genetics, researchers can generate improved predictions of their risk of
Read moreClemson University faculty have been awarded a grant from the National Institutes of Health to investigate the use of 3-D
Read moreParents of newborns may be familiar with the metabolic disorder phenylketonuria—in Switzerland, all newborn babies are screened for this genetic
Read moreGenetic testing can play a substantial role in medical management by uncovering changes in genes that are associated with an
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