LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z−) agrin-Reference-Cited by-同舟云学术

LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z−) agrin

Published:2011-12-29 Issue:7 Volume:131 Page:1123-1135
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Maselli Ricardo A.,Fernandez Jose M.,Arredondo Juan,Navarro Carmen,Ngo Maian,Beeson David,Cagney Órla,Williams D. Colette,Wollmann Robert L.,Yarov-Yarovoy Vladimir,Ferns Michael J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-011-1132-4.pdf

Reference43 articles.

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3. Bogdanik LP, Burgess RW (2011) A valid mouse model of AGRIN-associated congenital myasthenic syndrome. Hum Mol Genet. doi: 10.1093/hmg/ddr396

4. Burgess RW, Nguyen QT, Son YJ, Lichtman JW, Sanes JR (1999) Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction. Neuron 23(1):33–44

5. Burgess RW, Dickman DK, Nunez L, Glass DJ, Sanes JR (2002) Mapping sites responsible for interactions of agrin with neurons. J Neurochem 83(2):271–284

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