normal vision phenotype
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (5)
Papers in which this entity is mentioned.
- The Detection of Phase Amplitude Coupling during Sensory Processing. (2017)
- Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. (2014)
- Altering cortical connectivity: remediation-induced changes in the white matter of poor readers. (2009)
- Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. (2008)
- Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters. (2008)
Merged raw entities (2)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| normal vision | phenotype | 5 | 5 |
| normal or corrected to normal vision | phenotype | — | — |