|1.||Pattnaik, Bikash R: 2 articles (07/2015 - 01/2014)|
|2.||Edwards, Albert O: 2 articles (03/2013 - 12/2004)|
|3.||Liu, Xinying: 1 article (07/2015)|
|4.||Shahi, Pawan K: 1 article (07/2015)|
|5.||Pillers, De-Ann M: 1 article (07/2015)|
|6.||Brar, Simran: 1 article (07/2015)|
|7.||York, Nathaniel: 1 article (07/2015)|
|8.||Traboulsi, Elias I: 1 article (07/2015)|
|9.||Chiang, John: 1 article (07/2015)|
|10.||Marino, Meghan J: 1 article (07/2015)|
12/01/2004 - "To identify the chromosomal location of the gene causing snowflake vitreoretinal degeneration (SVD), an autosomal dominant retinal degeneration characterized by small yellow-white dots in the retina, fibrillar anomaly of the vitreous humor, and retinal detachment. "
03/01/2013 - "A mutation in KCNJ13 resulting in an arginine-to-tryptophan change at residue 162 (R162W) of Kir7.1 was associated with snowflake vitreoretinal degeneration, an inherited autosomal-dominant disease characterized by vitreous degeneration and mild retinal degeneration. "
|2.||Leber Congenital Amaurosis
|3.||Retinal Detachment (Retinal Detachments)
|4.||Blindness (Hysterical Blindness)
|1.||Inwardly Rectifying Potassium Channels (Inward Rectifier Potassium Channels)