Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

Arkadiusz Piotrowski, Jing Xie, Ying F. Liu, Andrzej B. Poplawski, Alicia R. Gomes, Piotr Madanecki, Chuanhua Fu, Michael R. Crowley, David K. Crossman, Linlea Armstrong, Dusica Babovic-Vuksanovic, Amanda Bergner, Jaishri Blakeley, Andrea L. Blumenthal, Molly S. Daniels, Howard Feit, Kathy Gardner, Stephanie Hurst, Christine Kobelka, Chung Lee & 8 others Rebecca Nagy, Katherine A. Rauen, John M. Slopis, Pim Suwannarat, Judith A. Westman, Andrea Zanko, Bruce R. Korf, Ludwine M. Messiaen

Research output: Contribution to journalArticle

Abstract

Constitutional SMARCB1 mutations at 22q11.23 have been found in ∼50% of familial and

Original languageEnglish (US)
Pages (from-to)182-187
Number of pages6
JournalNature Genetics
Volume46
Issue number2
DOIs
StatePublished - 2014

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Neurilemmoma
Mutation

ASJC Scopus subject areas

  • Genetics

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Piotrowski, A., Xie, J., Liu, Y. F., Poplawski, A. B., Gomes, A. R., Madanecki, P., ... Messiaen, L. M. (2014). Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. Nature Genetics, 46(2), 182-187. https://doi.org/10.1038/ng.2855

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. / Piotrowski, Arkadiusz; Xie, Jing; Liu, Ying F.; Poplawski, Andrzej B.; Gomes, Alicia R.; Madanecki, Piotr; Fu, Chuanhua; Crowley, Michael R.; Crossman, David K.; Armstrong, Linlea; Babovic-Vuksanovic, Dusica; Bergner, Amanda; Blakeley, Jaishri; Blumenthal, Andrea L.; Daniels, Molly S.; Feit, Howard; Gardner, Kathy; Hurst, Stephanie; Kobelka, Christine; Lee, Chung; Nagy, Rebecca; Rauen, Katherine A.; Slopis, John M.; Suwannarat, Pim; Westman, Judith A.; Zanko, Andrea; Korf, Bruce R.; Messiaen, Ludwine M.

In: Nature Genetics, Vol. 46, No. 2, 2014, p. 182-187.

Research output: Contribution to journalArticle

Piotrowski, A, Xie, J, Liu, YF, Poplawski, AB, Gomes, AR, Madanecki, P, Fu, C, Crowley, MR, Crossman, DK, Armstrong, L, Babovic-Vuksanovic, D, Bergner, A, Blakeley, J, Blumenthal, AL, Daniels, MS, Feit, H, Gardner, K, Hurst, S, Kobelka, C, Lee, C, Nagy, R, Rauen, KA, Slopis, JM, Suwannarat, P, Westman, JA, Zanko, A, Korf, BR & Messiaen, LM 2014, 'Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas', Nature Genetics, vol. 46, no. 2, pp. 182-187. https://doi.org/10.1038/ng.2855
Piotrowski, Arkadiusz ; Xie, Jing ; Liu, Ying F. ; Poplawski, Andrzej B. ; Gomes, Alicia R. ; Madanecki, Piotr ; Fu, Chuanhua ; Crowley, Michael R. ; Crossman, David K. ; Armstrong, Linlea ; Babovic-Vuksanovic, Dusica ; Bergner, Amanda ; Blakeley, Jaishri ; Blumenthal, Andrea L. ; Daniels, Molly S. ; Feit, Howard ; Gardner, Kathy ; Hurst, Stephanie ; Kobelka, Christine ; Lee, Chung ; Nagy, Rebecca ; Rauen, Katherine A. ; Slopis, John M. ; Suwannarat, Pim ; Westman, Judith A. ; Zanko, Andrea ; Korf, Bruce R. ; Messiaen, Ludwine M. / Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. In: Nature Genetics. 2014 ; Vol. 46, No. 2. pp. 182-187.
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