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Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2. (2018)

First Author: Laššuthová P

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/10.1111/cge.13417

PubMed Identifier: 30028002

Publication URI: http://europepmc.org/abstract/MED/30028002

Type: Journal Article/Review

Volume: 94

Parent Publication: Clinical genetics

Issue: 5

ISSN: 0009-9163