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Q54977127-3959D7F7-45F3-4633-B36A-BD56F232812B
Q54977127-3959D7F7-45F3-4633-B36A-BD56F232812B
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Statement
http://www.wikidata.org/entity/statement/Q54977127-3959D7F7-45F3-4633-B36A-BD56F232812B
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
Q54977127-3959D7F7-45F3-4633-B36A-BD56F232812B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-3959D7F7-45F3-4633-B36A-BD56F232812B
rank
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wasDerivedFrom
eada7336effc25426f074832c44b32c3ba913451
P2860
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency