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Q28299394-7BC8DA1F-247F-4319-BC4F-F92ABF803B76
Q28299394-7BC8DA1F-247F-4319-BC4F-F92ABF803B76
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http://www.wikidata.org/entity/statement/Q28299394-7BC8DA1F-247F-4319-BC4F-F92ABF803B76
Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature
P2860
Q28299394-7BC8DA1F-247F-4319-BC4F-F92ABF803B76
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28299394-7BC8DA1F-247F-4319-BC4F-F92ABF803B76
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wasDerivedFrom
d391a35dda268919f050a4a358462478c4527dbd
P2860
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome