Why are some genetic neuromuscular diseases still unsolved? The MYO-SEQ Project.

Last updated 10th Mar 2020
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A pinboard by Magdalena Mroczek

Research Assistant, Newcastle University


To perform genetic analysis on patients with limb-girdle muscle weakness from around the Europe

I am especially interested in limb girdle muscular dystrophies (LGMDs): a group of rare neuromuscular disorders characterised by weakness of the hip and shoulder muscles. There are approximately 30...