Expanding the mutational spectrum of LZTR1 in schwannomatosis-Reference-Cited by-同舟云学术

Expanding the mutational spectrum of LZTR1 in schwannomatosis

Published:2014-10-22 Issue:7 Volume:23 Page:963-968
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Paganini Irene,Chang Vivian Y,Capone Gabriele L,Vitte Jeremie,Benelli Matteo,Barbetti Lorenzo,Sestini Roberta,Trevisson Eva,Hulsebos Theo JM,Giovannini Marco,Nelson Stanley F,Papi Laura

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2014220.pdf

Reference29 articles.

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4. Plotkin SR, Blakeley JO, Evans DG et al: Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria. Am J Med Genet A 2013; 161A: 405–416.

5. Hulsebos TJ, Plomp AS, Wolterman RA, Robanus-Maandag EC, Baas F, Wesseling P . Germline mutation of INI1/SMARCB1 in familial schwannomatosis. Am J Hum Genet 2007; 80: 805–810.

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