Research shows mutation of the TMEM167A gene is responsible for the rare form of neonatal diabetes
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Research shows mutation of the TMEM167A gene is responsible for the rare form of neonatal diabetes
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The new technology, known as a hybrid closed loop system, will help reduce the risk of stillbirth and miscarriage
Discovery could revolutionise early identification and intervention for the deadly disease
A rare hereditary condition can elevate the risk of several kinds of cancer
Early trials have shown a massive reduction in seizures among young people with Dravet syndrome
New study raises urgent questions about how doctors treat diabetes
The potentially fatal condition affects one in every 3,000 babies
