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Atypical neurological symptoms associated with CGG expansions of theFMR1gene
Author(s) -
Esteban Peña
Publication year - 2013
Publication title -
world journal of neurology
Language(s) - English
Resource type - Journals
ISSN - 2218-6212
DOI - 10.5316/wjn.v3.i4.148
Subject(s) - fmr1 , medicine , gene , genetics , pediatrics , biology , fragile x

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