The results derived from our research have shed light into some of the most difficult questions about the genetics of the congenital myopathies. Our progress has been made possible in part thanks to the generosity of many families around the world who have participated in our research. Families enroll in our studies because they want to contribute to research, hoping that their participation may eventually benefit all individuals with neuromuscular disease. Our goals are to help all patients and their families by improving diagnostic methods and treatments for these disorders.
By clicking on the links on the left, you will be taken to pages with information about muscle disease and function, resources, our research, ways to help, and answers to frequently asked questions.
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