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P3‐149: DEMENTIA SYNDROME IN OCULOPHARYNGEAL MUSCULAR DYSTROPHY: A TRINUCLEOTIDE EXPANSION DISORDER COMMONLY PRESENTING WITH MUSCLE WEAKNESS
Author(s) -
Frederick Meredith C.,
Woltjer Randy,
Silbert Lisa C.,
Daniel Morad,
Nelson Adam A.,
Prince Carolyn,
ErtenLyons Deniz
Publication year - 2014
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2014.05.1238
Subject(s) - oculopharyngeal muscular dystrophy , frontotemporal dementia , dementia , trinucleotide repeat expansion , ptosis , medicine , compound heterozygosity , psychology , muscular dystrophy , genetics , psychiatry , disease , mutation , biology , surgery , allele , gene