Hereditary Diseases of the Retina
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-28956-4_36
Reference46 articles.
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3. Bech-Hansen NT, et al. Loss-of-function mutation in a calcium-channel alpha-subunit gene in Xp11.3 cause incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:264–7.
4. Bech-Hansen NT, et al. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nat Genet. 2000;26:319–23.
5. Berson EL. Retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1993;34:1659–76.
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