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Q54977127-61C870B9-B8B7-4CF3-81B1-D17045CD8739
Q54977127-61C870B9-B8B7-4CF3-81B1-D17045CD8739
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http://www.wikidata.org/entity/statement/Q54977127-61C870B9-B8B7-4CF3-81B1-D17045CD8739
A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
P2860
Q54977127-61C870B9-B8B7-4CF3-81B1-D17045CD8739
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Statement
http://www.wikidata.org/entity/statement/Q54977127-61C870B9-B8B7-4CF3-81B1-D17045CD8739
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wasDerivedFrom
eada7336effc25426f074832c44b32c3ba913451
P2860
Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy