Abnormal Electroretinogram after Kir7.1 Channel Suppression Suggests Role in Retinal Electrophysiology
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-11034-1.pdf
Reference51 articles.
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2. Leber, T. Ueber hereditare und congenitalangelegte Schnervenleiden. Graefes Arch Clin Exp Opthalmol, 249–291 (1871).
3. Cremers, F. P., van den Hurk, J. A. & den Hollander, A. I. Molecular genetics of Leber congenital amaurosis. Hum. Mol. Genet. 11, 1169–1176 (2002).
4. Weleber, R. G., Francis, P. J., Trzupek, K. M. & Beattie, C. In GeneReviews(R) (eds Pagon, R. A. et al.) (1993).
5. Sergouniotis, P. I. et al. Recessive mutations in KCNJ13, encoding an inwardly rectifying potassium channel subunit, cause leber congenital amaurosis. Am. J. Hum. Genet. 89, 183–190, doi: 10.1016/j.ajhg.2011.06.002 (2011).
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