Scientists track rare genetic disorder in families to unlock future treatments
NCT ID NCT01532791
Summary
This study aims to learn more about a rare genetic condition caused by a specific mitochondrial DNA mutation (m.3243A>G). Researchers will observe 300 participants, including people who carry the mutation and their family members, over time to understand the wide range of symptoms like migraines, seizures, and hearing loss. The study involves tests like MRIs, blood work, and questionnaires but does not provide any treatment.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Columbia University
RECRUITINGNew York, New York, 10032, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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