Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
15 auth.
N. BechâHansen,
M. Naylor,
T. Maybaum,
R. Sparkes,
B. Koop,
D. Birch,
A. Bergen,
C. Prinsen,
R. Polomeno,
A. Gal,
...
A. Drack,
M. Musarella,
S. Jacobson,
R. Young,
R. Weleber
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8 |
2000 |
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