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Limb-Girdle Muscular Dystrophy (LGMD)
The limb-girdle muscular dystrophy (LGMD) branch of the Rare Genomes Project is a partnership with the Muscular Dystrophy Association and the Jain Foundation dedicated to diagnosis and gene discovery through whole genome sequencing for individuals and families with LGMD.
Rare Genomes Project
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For Your Physician
The Rare Genomes Project is a research study at The Broad Institute of MIT and Harvard, a non-profit academic research institution focused on using genomic data to better understand human health and disease. Our team, led by investigator Heidi Rehm, has a specific focus on understanding the genetic...