UK10K
1. Congenital muscular dystrophies and congenital myopathies. 2. Neurogenic conditions. 3. Mitochondrial disorders. 4. Periodic paralysis. Conditions: No additional constraints. Data can be used as controls: Yes. Acknowledgement: The Molecular Genetics of Neuromuscular Disorders Study. UK10K_RARE_COLOBOMA. EGA Study ID: EGAS00001000127. ................
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