Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome (Q24626373)
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Language | Label | Description | Also known as |
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English | Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome |
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Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome (English)
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13 May 2011
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88
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650-6
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5
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