OPTN691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes

Title
OPTN691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes
Authors
Keywords
-
Journal
NEUROLOGY
Volume 86, Issue 5, Pages 446-453
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2016-01-07
DOI
10.1212/wnl.0000000000002334

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