Truncating
 SLC5A7
 mutations underlie a spectrum of dominant hereditary motor neuropathies

Claire G. Salter; Danique Beijer; Holly Hardy; Katy E.S. Barwick; Matthew Bower; Ines Mademan; Jonghe P De; Tine Deconinck; Mark A. Russell; Meriel M. McEntagart; Barry A. Chioza; Randy D. Blakely; John K. Chilton; Bleecker J De; Jonathan Baets; Emma L. Baple; David Walk; Andrew H. Crosby

doi:10.1212/nxg.0000000000000222

Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies

Claire G. Salter, Danique Beijer, Holly Hardy, Katy E.S. Barwick, Matthew Bower, Ines Mademan, Jonghe P De, Tine Deconinck, Mark A. Russell, Meriel M. McEntagart, Barry A. Chioza, Randy D. Blakely, John K. Chilton, Bleecker J De, Jonathan Baets, Emma L. Baple, David Walk, Andrew H. Crosby^*

^*Corresponding author for this work

Peninsula Medical School

Research output: Contribution to journal › Article › peer-review

Original language	English
Number of pages	0
Journal	Neurology Genetics
Volume	4
Issue number	2
DOIs	https://doi.org/10.1212/nxg.0000000000000222
Publication status	Published - Apr 2018

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10.1212/nxg.0000000000000222

Cite this

Salter, C. G., Beijer, D., Hardy, H., Barwick, K. E. S., Bower, M., Mademan, I., De, J. P., Deconinck, T., Russell, M. A., McEntagart, M. M., Chioza, B. A., Blakely, R. D., Chilton, J. K., De, B. J., Baets, J., Baple, E. L., Walk, D., & Crosby, A. H. (2018). Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies. Neurology Genetics, 4(2). https://doi.org/10.1212/nxg.0000000000000222

@article{42ed4e336cb74a42a2fe4a0e6d7d4a88,

title = "Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies",

author = "Salter, {Claire G.} and Danique Beijer and Holly Hardy and Barwick, {Katy E.S.} and Matthew Bower and Ines Mademan and De, {Jonghe P} and Tine Deconinck and Russell, {Mark A.} and McEntagart, {Meriel M.} and Chioza, {Barry A.} and Blakely, {Randy D.} and Chilton, {John K.} and De, {Bleecker J} and Jonathan Baets and Baple, {Emma L.} and David Walk and Crosby, {Andrew H.}",

year = "2018",

month = apr,

doi = "10.1212/nxg.0000000000000222",

language = "English",

volume = "4",

journal = "Neurology Genetics",

issn = "2376-7839",

number = "2",

}

Salter, CG, Beijer, D, Hardy, H, Barwick, KES, Bower, M, Mademan, I, De, JP, Deconinck, T, Russell, MA, McEntagart, MM, Chioza, BA, Blakely, RD, Chilton, JK, De, BJ, Baets, J, Baple, EL, Walk, D & Crosby, AH 2018, 'Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies', Neurology Genetics, vol. 4, no. 2. https://doi.org/10.1212/nxg.0000000000000222

TY - JOUR

T1 - Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies

AU - Salter, Claire G.

AU - Beijer, Danique

AU - Hardy, Holly

AU - Barwick, Katy E.S.

AU - Bower, Matthew

AU - Mademan, Ines

AU - De, Jonghe P

AU - Deconinck, Tine

AU - Russell, Mark A.

AU - McEntagart, Meriel M.

AU - Chioza, Barry A.

AU - Blakely, Randy D.

AU - Chilton, John K.

AU - De, Bleecker J

AU - Baets, Jonathan

AU - Baple, Emma L.

AU - Walk, David

AU - Crosby, Andrew H.

PY - 2018/4

Y1 - 2018/4

U2 - 10.1212/nxg.0000000000000222

DO - 10.1212/nxg.0000000000000222

M3 - Article

SN - 2376-7839

VL - 4

JO - Neurology Genetics

JF - Neurology Genetics

IS - 2

ER -