Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas-Reference-Cited by-同舟云学术

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

Published:2013-12-22 Issue:2 Volume:46 Page:182-187
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

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 O,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

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2855.pdf

Reference61 articles.

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2. Plotkin, S.R. et al. Update from the 2011 International Schwannomatosis Workshop: from genetics to diagnostic criteria. Am. J. Med. Genet. A. 161A, 405–416 (2013).

3. Smith, M.J. et al. Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis. Am. J. Med. Genet. A. 158A, 215–219 (2012).

4. Jacoby, L.B. et al. Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis. Am. J. Hum. Genet. 61, 1293–1302 (1997).

5. MacCollin, M. et al. Familial schwannomatosis: exclusion of the NF2 locus as the germline event. Neurology 60, 1968–1974 (2003).

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