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Neuroradiology|April 20, 2000
MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophyM Votruba, S Leary, N Losseff, et al.Biophysical Journal|September 2, 2000
Salt effects on ionization equilibria of histidines in myoglobinY H Kao, C A Fitch, S Bhattacharya, et al.Plos One|November 16, 2016
EYS Is a Protein Associated with the Ciliary Axoneme in Rods and ConesGiovanna Alfano, Przemyslaw M Kruczek, Amna Z Shah, et al.The West Indian Medical Journal|October 2, 2015
Time-dependent Degradation Pattern of Cardiac Troponin T in Cases of Death by BurnS Kumar, W Ali, U S Singh, et al.FEBS Letters|January 7, 1999
Induction of a spectroscopically defined transition by guanidinium hydrochloride on a recombinant calcium binding protein from Entamoeba histolyticaB Gopal, J V Krishna Rao, C J Thomas, et al.International Journal of Cosmetic Science|August 15, 2020
Emollient structure and chemical functionality effects on the biomechanical function of human stratum corneumC Berkey, D Kanno, A Mehling, et al.Drug and Alcohol Dependence|May 22, 2016
Benzylpiperazine: "A messy drug"D P Katz, J Deruiter, D Bhattacharya, et al.Ophthalmic Research|August 25, 2005
A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in British populationMohamed Farouk El-Ashry, Mai Mohamed Abd El-Aziz, Alison J Hardcastle, et al.American Journal of Human Genetics|October 1, 1996
Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotypeM Al-Maghtheh, E Vithana, E Tarttelin, et al.Human Mutation|April 3, 1999
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. OnlineD A Bessant, S Khaliq, A Hameed, et al.Pageof 144