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Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies

Title: Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies: .
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Name(s): Salter, Claire G., author
Beijer, Danique, author
Hardy, Holly, author
Barwick, Katy E.S., author
Bower, Matthew, author
Mademan, Ines, author
De Jonghe, Peter, author
Deconinck, Tine, author
Russell, Mark A., author
McEntagart, Meriel M., author
Chioza, Barry A., author
Blakely, Randy D., author
Chilton, John K., author
De Bleecker, Jan, author
Baets, Jonathan, author
Baple, Emma L., author
Walk, David, author
Crosby, Andrew H., author

, editor
, translator
Type of Resource: text
Genre: Article
Date Issued: 2018-04-23
Identifier: 10.1212/NXG.0000000000000222 (doi), flvc_fau_islandoraimporter_10.1212_NXG.0000000000000222_1634649520 (IID), http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000222 (uri)
Note(s):

Subject(s):
Persistent Link to This Record: http://purl.flvc.org/fau/flvc_fau_islandoraimporter_10.1212_NXG.0000000000000222_1634649520
Use and Reproduction: author
Host Institution: FAU
Is Part Of: Neurology Genetics.
, author
2376-7839