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Q58731949-28A6EEA1-60FF-4E9E-A1AB-8BF4C5DFA6B3
Q58731949-28A6EEA1-60FF-4E9E-A1AB-8BF4C5DFA6B3
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http://www.wikidata.org/entity/statement/Q58731949-28A6EEA1-60FF-4E9E-A1AB-8BF4C5DFA6B3
Structural analysis of the ternary complex between lamin A/C, BAF and emerin identifies an interface disrupted in autosomal recessive progeroid diseases
P2860
Q58731949-28A6EEA1-60FF-4E9E-A1AB-8BF4C5DFA6B3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58731949-28A6EEA1-60FF-4E9E-A1AB-8BF4C5DFA6B3
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wasDerivedFrom
74d7e2f6fa0f34333fcadee1b4e974b00d257b59
P2860
Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome.