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Q35127324-09688DBD-CCCA-48ED-81FA-624B0248320E
Q35127324-09688DBD-CCCA-48ED-81FA-624B0248320E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35127324-09688DBD-CCCA-48ED-81FA-624B0248320E
Fhl1 W122S causes loss of protein function and late-onset mild myopathy.
P2860
Q35127324-09688DBD-CCCA-48ED-81FA-624B0248320E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35127324-09688DBD-CCCA-48ED-81FA-624B0248320E
rank
NormalRank
type
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Statement
wasDerivedFrom
22407dc74a02caf4e0fb690344cdeae2b9d59651
P2860
Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.