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Items: 7

1.
A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxia
Imran H. Yusuf, Morag E Shanks, Penny Clouston, Robert E. MacLaren
Ophthalmic Genet. Author manuscript; available in PMC 2018 Oct 1.
Published in final edited form as: Ophthalmic Genet. 2018 Apr; 39(2): 263–267. Published online 2017 Dec 1. doi: 10.1080/13816810.2017.1408848
PMCID:
PMC5841564
ArticlePubReaderPDF–765KCite
2.
Heme and FLVCR-related transporter families SLC48 and SLC49
Anwar A. Khan, John G. Quigley
Mol Aspects Med. Author manuscript; available in PMC 2014 Apr 1.
Published in final edited form as: Mol Aspects Med. 2013 Apr; 34(2-3): 669–682. doi: 10.1016/j.mam.2012.07.013
PMCID:
PMC3602793
ArticlePubReaderPDF–972KCite
3.
Hereditary Ataxia: A Focus on Heme Metabolism and Fe-S Cluster Biogenesis
Deborah Chiabrando, Francesca Bertino, Emanuela Tolosano
Int J Mol Sci. 2020 Jun; 21(11): 3760. Published online 2020 May 26. doi: 10.3390/ijms21113760
PMCID:
PMC7312568
ArticlePubReaderPDF–1.2MCite
4.
Mutations in FLVCR1 Cause Posterior Column Ataxia and Retinitis Pigmentosa
Anjali M. Rajadhyaksha, Olivier Elemento, Erik G. Puffenberger, Kathryn C. Schierberl, Jenny Z. Xiang, Maria L. Putorti, José Berciano, Chantal Poulin, Bernard Brais, Michel Michaelides, Richard G. Weleber, Joseph J. Higgins
Am J Hum Genet. 2010 Nov 12; 87(5): 643–654. doi: 10.1016/j.ajhg.2010.10.013
PMCID:
PMC2978959
ArticlePubReaderPDF–1.3MCite
5.
A novel model for sustainable waste collection arc routing problem: Pareto-based algorithms
Erfan Babaee Tirkolaee, Alireza Goli, Selma Gütmen, Gerhard-Wilhelm Weber, Katarzyna Szwedzka
Ann Oper Res. 2023; 324(1-2): 189–214. Published online 2022 Jan 19. doi: 10.1007/s10479-021-04486-2
PMCID:
PMC8765820
ArticlePubReaderPDF–1.6MCite
6.
Potential Treatment of Retinal Diseases with Iron Chelators
Wanting Shu, Joshua L. Dunaief
Pharmaceuticals (Basel) 2018 Dec; 11(4): 112. Published online 2018 Oct 22. doi: 10.3390/ph11040112
PMCID:
PMC6316536
ArticlePubReaderPDF–648KCite
7.
Postmortem study of ataxia with retinitis pigmentosa by mutation of the α-tocopherol transfer protein gene
T Yokota, T Uchihara, J Kumagai, T Shiojiri, J Pang, M Arita, H Arai, M Hayashi, M Kiyosawa, R Okeda, H Mizusawa
J Neurol Neurosurg Psychiatry. 2000 Apr; 68(4): 521–525. doi: 10.1136/jnnp.68.4.521
PMCID:
PMC1736898
SummaryPDF–243KCite

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