Our mission is to improve the diagnosis, treatment and care of individuals with CACNA1C-related disorders...
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Neurofibromatosis type 1 (NF1) is a neurogenetic condition that approximately 1 in every 2,700 people...
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Usher syndrome (USH) is a rare, genetically inherited disease and its main symptoms are sensorineural...
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Wolfram Syndrome UK (WSUK) is the only charity and website in the UK for this...
Patient Groups / UK / 915 views / Popular