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Rare diseases, once considered medical curiosities, are now being increasingly recognised due to remarkable advancements in genomics, molecular biology, and diagnostic technologies. The completion of the Human Genome Project and subsequent research have revolutionised our understanding of human diseases. Despite this progress, the underlying genetic or phenotypic basis for many rare conditions remains poorly understood. More
Prof. Sarman Singh
MD, FRCP, FRSC, FRSTMH, FAMS, FABMS, FIMSA, FATP, FSIIP, FAAVR
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