Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy - Concepedia

Concepedia

Publication | Open Access

Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy

DOI Full Paper Access

13

Citations

8

References

2023

Year

Megan Soucy, Masha Kolesnikova, Angela H. Kim, Stephen H. Tsang

Documenta Ophthalmologica

BiologyMendelian DisorderGenetic DisorderGeneticsPhenotypic VariabilityDegenerative DiseaseMolecular GeneticsMedicineIncomplete Penetrance

References

	Year	Citations

Page 1