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