De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome (Q34326370)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome |
scientific article |
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De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome (English)
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James R Lupski
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Richard A Gibbs
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Donna M Muzny
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Yaping Yang
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Karen W Gripp
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Matthew N Bainbridge
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Hao Hu
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Luciana Musante
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Wei Chen
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Kim Jenny
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Thomas F Wienker
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V Reid Sutton
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H Hilger Ropers
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5 February 2013
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