Girl's deadly arrhythmia linked to mosaic of mutant cells
A team led by researchers at the Stanford University School of Medicine has solved a genetic mystery, diagnosing a sick baby and opening a new way for doctors to identify what might be causing genetic diseases with no obvious source.

Three years ago, when a newborn baby at Lucile Packard Children’s Hospital Stanford began going into cardiac arrest every few hours, doctors and nurses scrambled to save her life.
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