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Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma

Pasutto, F, Matsumoto, T, Mardin, C Y, Sticht, H, Brandstätter, J H, Michels-Rautenstrauss, K, Weisschuh, N, Gramer, E, Ramdas, W D, van Koolwijk, L M, Klaver, C C, Vingerling, J R, Weber, Bernhard H. F. , Kruse, F E, Rautenstrauss, B, Barde, Y-A and Reis, A (2009) Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma. The American Journal of Human Genetics 85 (4), pp. 447-456.

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Abstract

Glaucoma, a main cause of blindness in the developed world, is characterized by progressive degeneration of retinal ganglion cells (RGCs), resulting in irreversible loss of vision. Although members of the neurotrophin gene family in various species are known to support the survival of numerous neuronal populations, including RGCs, it is less clear whether they are also required for survival and ...

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Item type:Article
Date:2009
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1016/j.ajhg.2009.08.016DOI
19765683PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Partially
Item ID:35303
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