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Q36841149-ACCBE7A6-48C9-43EA-8284-D06514317DE6
Q36841149-ACCBE7A6-48C9-43EA-8284-D06514317DE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36841149-ACCBE7A6-48C9-43EA-8284-D06514317DE6
First Korean family with a mutation in TPM2 associated with Sheldon-Hall syndrome.
P2860
Q36841149-ACCBE7A6-48C9-43EA-8284-D06514317DE6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36841149-ACCBE7A6-48C9-43EA-8284-D06514317DE6
rank
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wasDerivedFrom
5a071380ac022f94bfccffa14e3936a12548eeb6
P2860
A myopathy-linked tropomyosin mutation severely alters thin filament conformational changes during activation.