Saturday 11 July 2020
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healtheuropa - 16 days ago

Genome sequencing: novel genetic cause of rare diseases discovered

A new study has discovered novel genetic causes of rare diseases which researchers believe could lead to the improvement of diagnosis and patient care. A UK National Institute for Health Research (NIHR) BioResource and Genomics England research programme is using genome sequencing in the NHS to diagnose hundreds of patients, leading to the new discovery [ ] The post Genome sequencing: novel genetic cause of rare diseases discovered appeared first on Health Europa.


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