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MDA’s award-winning bimonthly national magazine goes to everyone registered with MDA, as well as to MDA clinics, researchers and subscribers.
Quest publishes articles on all aspects of living with a neuromuscular disease, and updates on research findings. Quest’s circulation is 125,000.
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Check Out the New Digital Version of Quest! |
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Get Up, Get Out, Get Going
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Check out our selection of holiday gifts to enable and enhance your active lifestyle.
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Stories by Topic
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SPOTLIGHT ON GENE THERAPY AND MUSCLE
MD Human Trials will Target Membrane
Article Illustration:
When dystrophin (dark blue) is missing or diminished, Duchenne or Becker MD results. Loss of any of the sarcoglycans (yellow) leads to a limb-girdle type of MD. When laminin-2 (green) is lost, a disorder results that's known as congenital MD. The small adeno-associated virus can be sued to deliver genes for the sarcoglycans, while the larger adenovirus will be needed to transport genes for dystrophin or laminin-2.
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