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HADHA and HADHB gene associated phenotypes - Identification of rare variants in a patient cohort by Next Generation Sequencing. (2019)

First Author: Diebold I

Attributed to: Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.mcp.2019.01.003

PubMed Identifier: 30682426

Publication URI: http://europepmc.org/abstract/MED/30682426

Type: Journal Article/Review

Volume: 44

Parent Publication: Molecular and cellular probes

ISSN: 0890-8508