Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. (Q34313397)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. |
scientific article |
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Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. (English)
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Kailash Bhatia
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John Hardy
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Mark Tarnopolsky
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Delphine Héron
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Tobias B Haack
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Thomas Wieland
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Tim M Strom
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Penelope Hogarth
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Michael C Kruer
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Allison Gregory
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Thomas Schwarzmayr
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Stephan M Cuno
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Sami I Harik
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Vasuki H Dandu
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Nardo Nardocci
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Giovanna Zorzi
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Todd Dunaway
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Steven Skinner
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Era Hanspal
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Connie Schrander-Stumpel
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Cyril Mignot
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Manju A Kurian
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Susan J Hayflick
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Elisabeth Graf
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Lynn Sanford
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Esther Meyer
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Eleanna Kara
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Henry H Houlden
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21 November 2012
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