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See Latest ArticlesExpression of the diabetes risk gene wolframin (WFS1) in the human retina
Experimental Eye Research, 09/14/09
Schmidt–Kastner R et al. – Absence of these cells in the human specimens despite the use of human–specific antibodies to wolframin may be related to delayed fixation. Loss of wolframin function in RGCs and the unmyelinated portion of retinal axons could explain optic nerve atrophy in Wolfram Syndrome 1.
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