Whole Exome Sequencing Identifies TSC1/TSC2 Biallelic Loss as the Primary and Sufficient Driver Event for Renal Angiomyolipoma Development

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Veröffentlicht in:PLoS genetics 2016-08, Vol.12 (8), p.e1006242
Hauptverfasser: Giannikou, Krinio, Malinowska, Izabela A., Pugh, Trevor J., Yan, Rachel, Tseng, Yuen-Yi, Oh, Coyin, Kim, Jaegil, Tyburczy, Magdalena E., Chekaluk, Yvonne, Liu, Yang, Alesi, Nicola, Finlay, Geraldine A., Wu, Chin-Lee, Signoretti, Sabina, Meyerson, Matthew, Getz, Gad, Boehm, Jesse S., Henske, Elizabeth P., Kwiatkowski, David J.
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container_issue 8
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container_title PLoS genetics
container_volume 12
creator Giannikou, Krinio
Malinowska, Izabela A.
Pugh, Trevor J.
Yan, Rachel
Tseng, Yuen-Yi
Oh, Coyin
Kim, Jaegil
Tyburczy, Magdalena E.
Chekaluk, Yvonne
Liu, Yang
Alesi, Nicola
Finlay, Geraldine A.
Wu, Chin-Lee
Signoretti, Sabina
Meyerson, Matthew
Getz, Gad
Boehm, Jesse S.
Henske, Elizabeth P.
Kwiatkowski, David J.
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doi_str_mv 10.1371/journal.pgen.1006242
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title Whole Exome Sequencing Identifies TSC1/TSC2 Biallelic Loss as the Primary and Sufficient Driver Event for Renal Angiomyolipoma Development
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