Oculopharyngeal muscular dystrophy
Author:
Publisher
Elsevier
Reference108 articles.
1. Oculopharyngeal muscular dystrophy: recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies;Abu-Baker;Biochim Biophys Acta,2007
2. Involvement of the ubiquitin–proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy;Abu-Baker;Hum Mol Genet,2003
3. Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophy;Abu-Baker;Traffic,2005
4. The other trinucleotide repeat: polyalanine expansion disorders;Albrecht;Curr Opin Genet Dev,2005
5. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat Genet,2003
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