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Hypophosphatasia is a rare inherited metabolic disorder due to inactivating mutations of the ALPL-Gene. Particularly among adult patients, clinical manifestation exhibits a broad range of signs and sy...
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Lead Sponsor
Dr. Lothar Seefried
Collaborators
NCT07390240 · Hypophosphatasia
NCT05234567 · Hypophosphatasia
NCT07179640 · Hypophosphatasia (HPP)
NCT06079372 · Hypophosphatasia
NCT06015750 · Hypophosphatasia
Clinical Trial Unit, Orthopedic Department, Wuerzburg University
Würzburg
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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