Current Search: Hardy, Holly (x)
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Title
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Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies.
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Creator
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Salter, Claire G., Beijer, Danique, Hardy, Holly, Barwick, Katy E.S., Bower, Matthew, Mademan, Ines, De Jonghe, Peter, Deconinck, Tine, Russell, Mark A., McEntagart, Meriel M., Chioza, Barry A., Blakely, Randy D., Chilton, John K., De Bleecker, Jan, Baets, Jonathan, Baple, Emma L., Walk, David, Crosby, Andrew H.
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Date Issued
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2018-04-23
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PURL
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http://purl.flvc.org/fau/flvc_fau_islandoraimporter_10.1212_NXG.0000000000000222_1634649520
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Format
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Citation
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Title
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Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.
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Creator
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Wang, Haicui, Salter, Claire G, Refai, Osama, Hardy, Holly, Barwick, Katy E S, Akpulat, Ugur, Kvarnung, Malin, Chioza, Barry A, Harlalka, Gaurav, Taylan, Fulya, Sejersen, Thomas, Wright, Jane, Zimmerman, Holly H, Karakaya, Mert, Stüve, Burkhardt, Weis, Joachim, Schara, Ulrike, Russell, Mark A, Abdul-Rahman, Omar A, Chilton, John, Blakely, Randy D, Baple, Emma L, Cirak, Sebahattin, Crosby, Andrew H
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Date Issued
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2017-10-27
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PURL
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http://purl.flvc.org/fau/flvc_fau_islandoraimporter_10.1093_brain_awx249_1635361980
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Format
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Citation
