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Q50205993-782A6554-969F-4F05-853C-C284173AD101
Q50205993-782A6554-969F-4F05-853C-C284173AD101
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50205993-782A6554-969F-4F05-853C-C284173AD101
Autosomal dominant calpainopathy due to heterozygous CAPN3 c.643_663del21.
P2860
Q50205993-782A6554-969F-4F05-853C-C284173AD101
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50205993-782A6554-969F-4F05-853C-C284173AD101
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d5e5331977ce2584ebeb6dc6aebd554608b1a27c
P2860
Mutations in calpain 3 associated with limb girdle muscular dystrophy: analysis by molecular modeling and by mutation in m-calpain.