conference2011 jain-foundation.org

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Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant ALDA. Free Genetic Diagnosis for LGMDs. LGMD2BMiyoshi Myopathy collectively called dysferlinopathy are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective recessive inheritance. Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe.
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Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant ALDA. Free Genetic Diagnosis for LGMDs. LGMD2BMiyoshi Myopathy collectively called dysferlinopathy are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective recessive inheritance. Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe.

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The web page had the following in the site, "Automated LGMD Diagnostic Assistant ALDA." I saw that the web site stated " Free Genetic Diagnosis for LGMDs." They also said " LGMD2BMiyoshi Myopathy collectively called dysferlinopathy are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective recessive inheritance. Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe."

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