(Q43073577)
Statements
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Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome (English)
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M Plasilova
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C Chattopadhyay
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P Pal
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N A Schaub
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S A Buechner
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Hj Mueller
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P Miny
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A Ghosh
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K Heinimann
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1 August 2004
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41
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609-614
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Identifiers
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