Publications by authors named "Orly Agamy"

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VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2).
Miora Feinstein, Hagit Flusser, Tally Lerman-Sagie, Bruria Ben-Zeev, Dorit Lev, Orly Agamy

J Med Genet· May 2014

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Coding exons function as tissue-specific enhancers of nearby genes.
Ramon Y Birnbaum, E Josephine Clowney, Orly Agamy, Mee J Kim, Jingjing Zhao

Genome Res· June 2012

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Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy.
Orly Agamy, Bruria Ben Zeev, Dorit Lev, Barak Marcus, Dina Fine

Am J Hum Genet· October 2010

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