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Q28252989-424F92C7-5331-4A93-A50B-05A8289E0559
Q28252989-424F92C7-5331-4A93-A50B-05A8289E0559
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28252989-424F92C7-5331-4A93-A50B-05A8289E0559
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy
P2860
Q28252989-424F92C7-5331-4A93-A50B-05A8289E0559
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28252989-424F92C7-5331-4A93-A50B-05A8289E0559
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
874521129f9d9131aa1bd7aa24e11a1c76c39440
P2860
Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2