(Q46797092)
Statements
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A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features (English)
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Hilde Van Esch
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Anil K Agarwal
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Philippe Debeer
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Jean-Pierre Fryns
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Abhimanyu Garg
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8 November 2005
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91
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2
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517-521
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