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Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
2000
349 citations
Journal Article
Field-Weighted Citation Impact:
5.48
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness | Researchclopedia
Combined Ophthalmic Research Rotterdam
Clemens Prinsen
·
University of Calgary
Robert C. Polomeno
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McGill University
Andreas Gal
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Universität Hamburg
Arlene V. Drack
·
Emory Eye Center
Maria A. Musarella
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SUNY Downstate Health Sciences University
Samuel G. Jacobson
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University of Pennsylvania
Rockefeller S.L. Young
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Texas Tech University Health Sciences Center
Richard G. Weleber
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Oregon Health & Science University