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Q58731949-33D8A018-D4D3-4DD2-BA5C-D51213821BFA
Q58731949-33D8A018-D4D3-4DD2-BA5C-D51213821BFA
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Statement
http://www.wikidata.org/entity/statement/Q58731949-33D8A018-D4D3-4DD2-BA5C-D51213821BFA
Structural analysis of the ternary complex between lamin A/C, BAF and emerin identifies an interface disrupted in autosomal recessive progeroid diseases
P2860
Q58731949-33D8A018-D4D3-4DD2-BA5C-D51213821BFA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58731949-33D8A018-D4D3-4DD2-BA5C-D51213821BFA
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wasDerivedFrom
74d7e2f6fa0f34333fcadee1b4e974b00d257b59
P2860
Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy