Whole exome sequencing identifies de novo heterozygous CAV1 mutations associated with a novel neonatal onset lipodystrophy syndrome. (Q53535056)
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scientific article published on 21 April 2015
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English | Whole exome sequencing identifies de novo heterozygous CAV1 mutations associated with a novel neonatal onset lipodystrophy syndrome. |
scientific article published on 21 April 2015 |
Statements
Whole exome sequencing identifies de novo heterozygous CAV1 mutations associated with a novel neonatal onset lipodystrophy syndrome. (English)
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University of Washington Center for Mendelian Genomics
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Abhimanyu Garg
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Miguel Del Campo
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R Stephen Amato
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Anil K Agarwal
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21 April 2015
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167A
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8
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1796-1806
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