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article · 2017

Molecular defects identified by whole exome sequencing in a child with atypical mucopolysaccharidosis IIIB

Our results describe an atypical form of MPS IIIB and illustrate the diagnostic potential of targeted WES in Mendelian disease with unknown etiology. WES cou...

16 citationsDOI: https://doi.org/10.1515/jpem-2016-0333
Molecular defects identified by whole exome sequencing in a child with atypical mucopolysaccharidosis IIIB