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Town and Gown 10k event set for 42nd year in Oxford

These little girls were born with the same cruel genetic illness... but baby Amelia will never suffer like big sister Maisie - thanks to a miracle £75,000-a-dose jab

Portia Thorman of the Spinal Muscular Atrophy charity SMA, said these new treatments were not available when her son Ezra, pictured left, was born.

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New Advancement Toward The First Primary Endpoint Qualification Of A Digital Endpoint For Duchenne

Current methods for assessing ambulatory function in patients with Duchenne muscular dystrophy do not fully reflect how they experience DMD in their.

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