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Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature. (2019)

First Author: Savasta S

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1055/s-0038-1676603

PubMed Identifier: 31061755

Publication URI: http://europepmc.org/abstract/MED/31061755

Type: Journal Article/Review

Volume: 8

Parent Publication: Journal of pediatric genetics

Issue: 2

ISSN: 2146-460X