Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy. (Q30833220)

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Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy.
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    Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy (English)

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