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Q37015525-19A8A69A-7E2D-4EED-A946-8EA46E2DC5F5
Q37015525-19A8A69A-7E2D-4EED-A946-8EA46E2DC5F5
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http://www.wikidata.org/entity/statement/Q37015525-19A8A69A-7E2D-4EED-A946-8EA46E2DC5F5
Mutation-specific effects on thin filament length in thin filament myopathy.
P2860
Q37015525-19A8A69A-7E2D-4EED-A946-8EA46E2DC5F5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37015525-19A8A69A-7E2D-4EED-A946-8EA46E2DC5F5
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wasDerivedFrom
066000bfa4b3d9bdd5fb801e53c18fbc3c8328b9
P2860
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.