Publications by authors named "Miora Feinstein"

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A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13-q21.3.
Daniel Halperin, Nadav Agam, Maher Hallak, Miora Feinstein, Max Drabkin

Clin Genet· August 2022

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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

J Med Genet· May 2014

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Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.
Miora Feinstein, Barak Markus, Iris Noyman, Hannah Shalev, Hagit Flusser

Am J Hum Genet· December 2010

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