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You searched for: Author/Creator Webster, Richard

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1. Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. (4th October 2016)

3. Auditory neuropathy in Brown–Vialetto–Van Laere syndrome due to riboflavin transporter RFVT2 deficiency. (25th February 2016)

5. Characterization of an anti-fetal AChR monoclonal antibody isolated from a myasthenia gravis patient. Issue 1 (December 2017)

8. New Miscanthus hybrids cultivated at a Polish metal-contaminated site demonstrate high stomatal regulation and reduced shoot Pb and Cd concentrations. (September 2019)

9. Assembly of cerium-based coordination polymer into variant polycrystalline 2D–3D CeO2−x nanostructures. Issue 9 (14th January 2020)

10. Eye movement disorders are an early manifestation of CACNA1A mutations in children. (27th January 2016)