Scientists hunt for genetic clues to rare muscle disorders
NCT ID NCT00272883
Summary
This research program aims to better understand the genetic causes of congenital myopathies—rare muscle disorders present from birth. Researchers are studying DNA from 4,000 participants worldwide to identify genes involved in these conditions. The goal is to improve future diagnosis and treatment by connecting genetic findings with patients' symptoms.
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Study contacts
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Contact
Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Genetics Division, Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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