fukutin protein

A global registry has been launched for people with conditions caused by mutations in the FKRP gene, such as LGMD2I and CMD1C

posted on August 19, 2011 - 2:51pm
A new registry has been launched for people with conditions caused by mutations in the gene for fukutin-related protein (FKRP). This includes people with the type 2I form of limb-girdle muscular dystrophy (LGMD) and the type 1C form of congenital muscular dystrophy (CMD) and, in rare instances, the congenital muscular dystrophies muscle-eye-brain disease and Walker-Warburg syndrome.

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