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TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies

Klein, CJ; Shi, Y; Fecto, F; Donaghy, M; Nicholson, G; McEntagart, ME; Crosby, AH; Wu, Y; Lou, H; McEvoy, KM; et al. Klein, CJ; Shi, Y; Fecto, F; Donaghy, M; Nicholson, G; McEntagart, ME; Crosby, AH; Wu, Y; Lou, H; McEvoy, KM; Siddique, T; Deng, HX; Dyck, PJ (2011) TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies. NEUROLOGY, 76 (10). 887 - 894 (8). ISSN 0028-3878 https://doi.org/10.1212/WNL.0b013e31820f2de3
SGUL Authors: Crosby, Andrew Harry McEntagart, Meriel

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Item Type: Article
Additional Information: PubMed ID: 21288981
Keywords: Adult, Amino Acids, Animals, Axons, Calcium, Cell Line, Transformed, Cell Survival, Charcot-Marie-Tooth Disease, Diaphragm, Family Health, Humans, Hypercalcemia, Intracellular Fluid, Male, Mutation, Ruthenium Red, TRPV Cation Channels, Transfection, Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, SENSORY NEUROPATHY, HEREDITARY MOTOR, PARKINSONS-DISEASE, CELL-DEATH, CALCIUM, CORD, DISORDERS, HMSN2C, MODEL, GENE
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: NEUROLOGY
ISSN: 0028-3878
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Dates:
DateEvent
1 March 2011Published
Web of Science ID: WOS:000288117500010
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URI: http://openaccess.sgul.ac.uk/id/eprint/352
Publisher's version: https://doi.org/10.1212/WNL.0b013e31820f2de3

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