Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity. (2020)
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.jmoldx.2020.06.008
PubMed Identifier: 32619640
Publication URI: http://europepmc.org/abstract/MED/32619640
Type: Journal Article/Review
Volume: 22
Parent Publication: The Journal of molecular diagnostics : JMD
Issue: 9
ISSN: 1525-1578