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Study uncovers rare genetic syndrome caused by mutations in gene SATB1 – News-Medical.net
Advances in DNA sequencing have uncovered a rare syndrome which is caused by variations in the gene SATB1.
Advances in DNA sequencing have uncovered a rare syndrome which is caused by variations in the gene SATB1.
The study, co-authored by academics from Oxford Brookes University (UK), University of Lausanne (Switzerland), Radboud University (The Netherlands), University of Oxford (UK), University of Manchester (UK) and led by Max Planck Institute for Psycholinguistics (The Netherlands), discovered three classes of mutations within the gene SATB1, resulting in three variations of a neurodevelopmental…
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