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Neuro-Ophthalmology Volume 41, 2017 - Issue 5
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Case Reports

Three New PAX2 Gene Mutations in Patients with Papillorenal Syndrome

Alberto Galvez-RuizKing Khaled Eye Specialist Hospital, Riyadh, Saudi ArabiaCorrespondence[email protected]
,
Anthony J. LehnerOrthoptic Division, Vision Eye Institute, New South Wales, Australia
,
Alicia Galindo-FerreiroKing Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia
&
Patrik SchatzKing Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia;Department of Ophthalmology, Department of Clinical Sciences, Scane County University Hospital, University of Lund, Lund, SwedenORCID Iconhttp://orcid.org/0000-0002-1747-0928
ORCID Icon
Pages 271-278 | Received 26 Feb 2017, Accepted 14 Mar 2017, Published online: 08 May 2017

Citations (5)

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Read on this site (1)

Na Lv, Ying Wang, Min Zhao, Lina Dong & Hongen Wei. (2021) The Role of PAX2 in Neurodevelopment and Disease. Neuropsychiatric Disease and Treatment 17, pages 3559-3567.
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Articles from other publishers (4)

Na Lv, Ying Wang, Yongfeng Liu, Jiaming Tang, Qiang Lei, Yizhuo Wang & Hongen Wei. (2022) Decreased Microglia in Pax2 Mutant Mice Leads to Impaired Learning and Memory . ACS Chemical Neuroscience 13:16, pages 2490-2502.
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Bei Liu, Mengjia Chen, Yanmei Yang, Yingzhi Huang, Yeqing Qian & Minyue Dong. (2022) Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings. Clinica Chimica Acta 525, pages 23-28.
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Ruibao Liu, Wenyuan Jian, Ying Zhao, Xuejing Lu, Yanxia Wu & Junguo Duan. (2020) Retinal oxygen saturation and vessel diameter in patients with chronic kidney disease. Acta Ophthalmologica 99:3.
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Jessica Maria Forero-Delgadillo, Vanessa Ochoa, Natalia Duque, Jaime Manuel Restrepo, Hernando Londoño, Jose Antonio Nastasi-Catanese & Harry Pachajoa. (2021) New PAX2 Mutation Associated with Polycystic Kidney Disease: A Case Report. Clinical Medicine Insights: Pediatrics 15, pages 117955652199235.
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