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Manchester Rare Conditions Centre Partners with Medics for Rare Disease to Enhance Training for Healthcare Professionals.
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Acute-onset axonal neuropathy following infection in children with biallelic RCC1 variants
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Ectodermal Dysplasia Rare Disease Collaborative Network (RDCN)
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R-loop-associated snRNA gene variants implicated in neurodevelopmental disorders
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Update on the management guidelines for Kabuki Syndrome
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MRCC at the 2025 Cure CLCN4 Scientific Conference
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Unique Guides using AI – Call to Clinicians
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Manchester-led research finds genetic causes of rare condition linked to hearing loss and infertility
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We R Rare
We R Rare Meeting – 4th February 2025
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