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

Last updated 10th Mar 2020
Follow pinboard

CURATOR

A pinboard by Magdalena Mroczek

Research Assistant, Newcastle University

PINBOARD SUMMARY

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...