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Q28252989-8677AB61-E601-4204-91E8-773298388051
Q28252989-8677AB61-E601-4204-91E8-773298388051
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28252989-8677AB61-E601-4204-91E8-773298388051
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy
P2860
Q28252989-8677AB61-E601-4204-91E8-773298388051
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28252989-8677AB61-E601-4204-91E8-773298388051
rank
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type
BestRank
Statement
wasDerivedFrom
874521129f9d9131aa1bd7aa24e11a1c76c39440
P2860
Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)