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Last updated in GTR:
At a Glance
Autosomal recessive centronuclear myopathy; Central core disease; Congenital myopathy more...
ACTA1 (1q42.13); BIN1 (2q14.3); CCDC78 (16p13.3); CFL2 (14q13.1); CNTN1 (12q12) more...
Conditions Help
Total conditions: 20
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
Instrument *
* Instrument: Not provided
Technical Information
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Additional Information

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