Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness - Concepedia

Concepedia

Publication | Closed Access

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

349

Citations

23

References

2000

Year

N. Torben Bech‐Hansen, Margaret J. Naylor, Tracy A. Maybaum, Rebecca Sparkes, Ben F. Koop, David G. Birch, Arthur A. Bergen, Clemens Prinsen, Robert C. Polomeno, Andreas Gal,

Nature Genetics

Ocular DiseaseDevelopmental BiologyOphthalmologyPathologyPediatric OphthalmologyLeucine-rich Proteoglycan NyctalopinOcular PathologyMedicineNeurogenetics

References

	Year	Citations

Page 1

Page 1