Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome (Q24626373)

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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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    Victor Quesada
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    Juan Cadiñanos
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    Julia M Fraile
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    Miriam Fanjul-Fernández
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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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