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Q40492542-1F7E918E-5FC1-47DB-9E64-DE2022A650F7
Q40492542-1F7E918E-5FC1-47DB-9E64-DE2022A650F7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40492542-1F7E918E-5FC1-47DB-9E64-DE2022A650F7
Clinical utility gene card for: Multi-minicore disease.
P2860
Q40492542-1F7E918E-5FC1-47DB-9E64-DE2022A650F7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40492542-1F7E918E-5FC1-47DB-9E64-DE2022A650F7
rank
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Statement
wasDerivedFrom
dc84617ac088f77827a7cffb98fc21786f278a97
P2860
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.