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
Related URLs:	Author
Dates:	Date Event 1 March 2011 Published
Web of Science ID:	WOS:000288117500010
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URI:	https://openaccess.sgul.ac.uk/id/eprint/352
Publisher's version:	https://doi.org/10.1212/WNL.0b013e31820f2de3

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