Whole genome sequencing increases diagnosis of rare disorders by nearly a third, study finds
Study reveals ‘extensive network’ of industry ties with healthcare
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4 November 2021Whole genome sequencing increases diagnosis of rare disorders by nearly a third, study finds
Mitochondrial disorders affect around 1 in 4300 people and cause progressive, incurable diseases. They are amongst the most common inherited diseases but are difficult for clinicians to diagnose, not least because they can affect many different organs and resemble many other conditions.
