hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes

标题
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes
作者
关键词
-
出版物
NEUROBIOLOGY OF AGING
Volume 35, Issue 4, Pages 934.e5-934.e6
出版商
Elsevier BV
发表日期
2013-10-09
DOI
10.1016/j.neurobiolaging.2013.09.016

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