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Pilot launched to support children with rare conditions to access personalised therapies

Genomics England November 22, 2023 New programme announced to develop a pathway for children with rare conditions to access therapies...

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Clinician (physician

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Patient

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General interest

Patient identification and selection

Trial implementation

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What brought you to the N=1 Collaborative? What are you hoping to gain, contribute, learn, or participate in?

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501c3 Nonprofit Organization

EIN: 88-2591503

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