NIHR BioResource – Rare Diseases – Issue February: 2018
The National Institute for Health Research (NIHR) BioResource – Rare Diseases was established in 2012 with the intention of engaging with patients with rare diseases and their family members, who consent to be contacted and invited to participate in medical research studies. Those who joined the BioResource have provided a sample of blood or saliva and DNA from 13 ,000 samples have been sent for whole-genome sequencing…
If you would like to find out how our recent Rare Disease “Think Research” event went, please click here.
Find out more
If you would like to find out further information about the NIHR BioResource, please click the link below, to find the person to direct your enquiries to.