Cure CMD announces CMD BioBank

To find treatments for the CMDs and identify new CMD genes requires support from the CMD community. If you have CMD or are a sibling or parent of someone with CMD, we would like you to consider supporting CMD Discovery through donating a blood or skin biopsy sample to the CMD BioBank located at the NIGMD respository at the Coriell Medical Institute.

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  • Congenital Muscular Dystrophy

    A group of diseases causing muscle weakness at birth. Several defined genetic mutations cause muscles to break down faster than they can repair or grow. A child with CMD may have various neurological or physical impairments. Some children never gain the ability to walk, while others lose the ability as they grow older. Learn more...

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