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Q39072434-2566303C-AE3E-45F1-B8DB-F99AC410A2E1
Q39072434-2566303C-AE3E-45F1-B8DB-F99AC410A2E1
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http://www.wikidata.org/entity/statement/Q39072434-2566303C-AE3E-45F1-B8DB-F99AC410A2E1
Lamin A Δexon9 mutation leads to telomere and chromatin defects but not genomic instability.
P2860
Q39072434-2566303C-AE3E-45F1-B8DB-F99AC410A2E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39072434-2566303C-AE3E-45F1-B8DB-F99AC410A2E1
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wasDerivedFrom
1af684d73439b904ad24c78f999ef8ce1bfb2f07
P2860
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome