Cottenie, E.
51  results:
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3

P41 Genetic analysis of FIG4 in patients with CMT:

Cottenie, E. ; Laurá, M. ; Hanna, M....
Neuromuscular Disorders.  22 (2012)  - p. S18 , 2012
 
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Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilam..:

Rebelo, AP ; Abrams, AJ ; Cottenie, E...
https://discovery.ucl.ac.uk/id/eprint/1481244/1/Holton_NEFH%20final2.pdf.  , 2016
 
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6

Genetic and functional investigation of inherited neuropath..:

Cottenie, E
https://discovery.ucl.ac.uk/id/eprint/1472571/1/Viva%20Ellen%20Cottenie_corrected%20version.pdf.  , 2015
 
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7

Truncating and missense mutations in IGHMBP2 cause Charcot-..:

Cottenie, E ; Kochanski, A ; Jordanova, A...
https://discovery.ucl.ac.uk/id/eprint/1457906/1/mmc2.pdf.  , 2014
 
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Mutations in gamma adducin are associated with inherited ce..:

Kruer, MC ; Jepperson, T ; Dutta, S...
https://discovery.ucl.ac.uk/id/eprint/1413050/1/ana23971.pdf.  , 2013
 
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13

Into the wild: microbiome transplant studies need broader e..:

Greyson-Gaito, Christopher J. ; Bartley, Timothy J. ; Cottenie, Karl...
Proceedings of the Royal Society B: Biological Sciences.  287 (2020)  1921 - p. 20192834 , 2020
 
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