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Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma

✍ Scribed by P. Corcia; J. Praline; A.M. Guennoc; R.A. Thépault; P.H. Gordon; H. Blasco; C.R. Andres; P. Vourc'h

Book ID: 119304229
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 116 KB
Volume: 309
Category: Article
ISSN: 0022-510X
DOI: 10.1016/j.jns.2011.07.044

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