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The goal of this Natural History Study for Charcot-Marie-Tooth is to acquire, record, and analyze patient-reported data and associated genetic reports, Electronic Health Records (EHRs) and clinical no...
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Lead Sponsor
Hereditary Neuropathy Foundation
NCT06794489 · CMT1A, CMT (Charcot Marie Tooth Disease), and more
NCT03047369 · Leukodystrophy, White Matter Disease, and more
NCT01193088 · Charcot-Marie-Tooth Disease, Type Ia (Disorder), HMSN
NCT07049588 · Charcot-Marie-Tooth Disease Type 1A
NCT06881979 · Amyotrophic Lateral Sclerosis, Chronic Inflammatory Demyelinating Neuropathy, and more
Hereditary Neuropathy Foundation
New York, New York
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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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