Pigmentary maculopathy in a patient with Wolfram syndrome.
about
Expression of the diabetes risk gene wolframin (WFS1) in the human retina.Wolfram syndrome: important implications for pediatricians and pediatric endocrinologists.The Eye on Mitochondrial Disorders.Retinal thickness as a marker of disease progression in longitudinal observation of patients with Wolfram syndrome.
P2860
Pigmentary maculopathy in a patient with Wolfram syndrome.
description
2006 nî lūn-bûn
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name
Pigmentary maculopathy in a patient with Wolfram syndrome.
@en
Pigmentary maculopathy in a patient with Wolfram syndrome.
@nl
type
label
Pigmentary maculopathy in a patient with Wolfram syndrome.
@en
Pigmentary maculopathy in a patient with Wolfram syndrome.
@nl
prefLabel
Pigmentary maculopathy in a patient with Wolfram syndrome.
@en
Pigmentary maculopathy in a patient with Wolfram syndrome.
@nl
P2093
P1476
Pigmentary maculopathy in a patient with Wolfram syndrome.
@en
P2093
Daniel S Zuckerbrod
Mandeep S Dhalla
Uday R Desai
P356
10.1016/S0008-4182(06)80064-5
P577
2006-02-01T00:00:00Z