Combinatorial treatment increases IKAP levels in human cells generated from Familial Dysautonomia patients
Author:
Funder
Israel Science Foundation
Teva Pharmaceutical Industries
Dysautonomia Foundation
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference66 articles.
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2. Familial dysautonomia: History, genotype, phenotype and translational research;L Norcliffe-Kaufmann;Prog Neurobiol,2017
3. Familial Dysautonomia: Mechanisms and Models;P Dietrich;Genet Mol Biol,2016
4. Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia;SA Slaugenhaupt;Am J Hum Genet,2001
5. Familial dysautonomia is caused by mutations of the IKAP gene;SL Anderson;Am J Hum Genet,2001
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