Improving the clinical interpretation of missense variants in X linked genes using structural analysis. (2022)
Attributed to:
Interpretation of genomic sequencing for inherited ophthalmic disease: an integrated approach
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2020-107404
PubMed Identifier: 33766936
Publication URI: http://europepmc.org/abstract/MED/33766936
Type: Journal Article/Review
Volume: 59
Parent Publication: Journal of medical genetics
Issue: 4
ISSN: 0022-2593