The Genetics Podcast

EP 16 Policy Development and Patient Engagement for Rare Disease with Alistair Kent

September 6th, 2019  •  1 hr 7 mins  •  Download (77.6 MB)  •  Link with Timestamp

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This week on our podcast, we speak to Alastair Kent, a world leader in policy development and patient engagement for rare disease. In this episode, we discuss how research is changing in rare conditions and what part DNA sequencing and data sharing...