Thursday 9 July 2020
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healtheuropa - 2 month ago

Mutation discovery could lead to treatment for rare neurological disorder

A team of researchers have discovered a mutation in a protein that can cause a rare neurological disorder – leading to the identification of a possible treatment. Biochemist Edwin Chapman and his team have figured out how mutations in one protein, called synaptotagmin-1 or syt1, can lead to a rare neurological disorder known as syt1-associated [ ] The post Mutation discovery could lead to treatment for rare neurological disorder appeared first on Health Europa.


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