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Journal of Medical Genetics logoLink to Journal of Medical Genetics
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. 2004 Aug;41(8):609–614. doi: 10.1136/jmg.2004.019661

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

M Plasilova, C Chattopadhyay, P Pal, N Schaub, S Buechner, H Mueller, P Miny, A Ghosh, K Heinimann
PMCID: PMC1735873  PMID: 15286156

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