Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar (2020)
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/10.1038/s41431-020-0623-y
PubMed Identifier: 32313206
Publication URI: http://europepmc.org/abstract/MED/32313206
Type: Journal Article/Review
Parent Publication: European Journal of Human Genetics
Issue: 9
ISSN: 1018-4813