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SPINAL MUSCULAR ATROPHY
'India’s Got Latent' Row: SC Seeks Samay Raina, Other Social Media Influencers’ Presence in Court for ‘Ridiculing’ Disabled
Spinal Muscular Atrophy Drugs: Can Medicine for Rare Disorder SMA Be Made Available at Lower Price in India, Supreme Court to Drug Manufacturer
Spinal Muscular Atrophy Injection for Toddler: AAP’s Sanjay Singh Appeals People to Contribute for Injection Worth Rs 17 Crore for 16-Month-Old Child
Zolgensma Injection: All You Need To Know About Rs 17 Crore Jab for Spinal Muscular Atrophy
Rajasthan: 2-Year-Old Boy Suffering From Spinal Muscular Atrophy Dies at Jaipur Hospital As Family Waited in Vain for Rs 16 Crore Injection
Spinal Muscular Atrophy: 23-Month-Old Baby Ellen With Rare Genetic Disease Administered Rs 16 Crore Drug in Telangana
Pune: Vedika Shinde, Baby Girl Who Was Diagnosed with SMA Type-1 And Received Rs 16 Crore Injection, Dies
Tanishk Singh, 10-Month-Old Suffering From Rare Genetic Disorder, Needs Injection Worth Rs 16 Crore, Parents Pin Their Hope on Crowdfunding To Save His Life
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