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24-hydroxylase Deficiency clinical trials

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NCT ID: NCT03478761 Recruiting - Clinical trials for 24-hydroxylase Deficiency

24-Hydroxylase Deficiency and CYP24A1 Mutation Patient Registry

Start date: October 19, 2017
Study type: Observational [Patient Registry]

You are being asked to take part in this research registry because you or your family member is suspected to have a 24-hydroxylase deficiency.