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Fukuyama congenital muscular dystrophy
- Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are ...
- Walker-Warburg syndrome is an inherited disorder that affects development of the muscles, brain, and eyes. It is the most severe of a group of genetic conditions ...
- ... the FKTN gene have been found to cause Fukuyama congenital muscular dystrophy, a condition that causes skeletal muscle weakness and ... and function of skeletal muscles in people with Fukuyama congenital muscular dystrophy.Defective α-dystroglycan also affects the migration of ...
- ... the POMT1 gene have been found to cause Walker-Warburg syndrome, the most severe form of a group of disorders known as congenital muscular dystrophies. Individuals with Walker-Warburg syndrome have skeletal muscle weakness and abnormalities of the ...
- ... the POMT2 gene have been found to cause Walker-Warburg syndrome. This condition is the most severe form of ... group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes muscle weakness and abnormalities of the brain ...
- ... the CRPPA gene have been found to cause Walker-Warburg syndrome, the most severe form of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the ...
- ... the LARGE1 gene have been found to cause Walker-Warburg syndrome. This condition is the most severe form of ... group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the ...
- ... the FKRP gene have been found to cause Walker-Warburg syndrome. This condition is the most severe form of ... group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and abnormalities of the ...