The obtained results expanded mutational and phenotype spectrum of β-crystallin genes and offer clues for pathogenesis of congenital cataracts. The data also demonstrated that targeted exome sequencing is valuable for providing molecular diagnostic information for congenital cataract patients.
Keyphrases
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- prognostic factors
- electronic health record
- peritoneal dialysis
- single cell
- healthcare
- genome wide
- cancer therapy
- machine learning
- patient reported outcomes
- copy number
- drug delivery
- social media
- transcription factor
- artificial intelligence