Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Optic Atrophy and MFN2[original query] |
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Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study. BMC medical genetics 2009 10 91. Wolf Christiane, Gramer Eugen, Müller-Myhsok Bertram, Pasutto Francesca, Reinthal Eva, Wissinger Bernd, Weisschuh Nico |
Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2. Journal of neurology 2011 1 258 (7): 1234-9. McCorquodale Donald S, Montenegro Gladys, Peguero Ainsley, Carlson Nicole, Speziani Fiorella, Price Justin, Taylor Sean W, Melanson Michel, Vance Jeffery M, Züchner Steph |
Association between Mitofusin 2 Gene Polymorphisms and Late-Onset Alzheimer's Disease in the Korean Population. Psychiatry investigation 2017 Jan 14 (1): 81-85. Kim Young Jong, Park Jin Kyung, Kang Won Sub, Kim Su Kang, Han Changsu, Na Hae Ri, Park Hae Jeong, Kim Jong Woo, Kim Young Youl, Park Moon Ho, Paik Jong-W |
Optic Neuropathy in Charcot-Marie-Tooth Disease. Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2020 5 41 (2): 233-238. Hamedani Ali G, Wilson James A, Avery Robert A, Scherer Steven |
Associations between OPA1, MFN1, and MFN2 polymorphisms and primary open angle glaucoma in Polish participants of European ancestry. Ophthalmic genetics 2021 Aug 1-6. Milanowski Piotr, Kosior-Jarecka Ewa, ?ukasik Urszula, Wróbel-Dudzi?ska Dominika, Milanowska Joanna, Khor Chiea Chuen, Aung Tin, Kocki Janusz, ?arnowski Toma |
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