Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.

C.M. Westermann; L. Dorland; D.M. Votion; M.G.M. de Sain - van der Velden; I.D. Wijnberg; R.J.A. Wanders; W.G.M. Spliet; N. Testerink; R. Berger; J.P.N. Ruiter; J.H. van der Kolk

doi:10.1016/j.nmd.2008.02.007

Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.

Translated title of the contribution: Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.

C.M. Westermann, L. Dorland, D.M. Votion, M.G.M. de Sain - van der Velden, I.D. Wijnberg, R.J.A. Wanders, W.G.M. Spliet, N. Testerink, R. Berger, J.P.N. Ruiter, J.H. van der Kolk

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

Translated title of the contribution	Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
Original language	Undefined/Unknown
Pages (from-to)	355-364
Number of pages	10
Journal	Neuromuscular Disorders
Volume	18
Issue number	5
DOIs	https://doi.org/10.1016/j.nmd.2008.02.007
Publication status	Published - 2008

Keywords

Econometric and Statistical Methods: General
Geneeskunde(GENK)

Access to Document

10.1016/j.nmd.2008.02.007

Cite this

Westermann, C. M., Dorland, L., Votion, D. M., de Sain - van der Velden, M. G. M., Wijnberg, I. D., Wanders, R. J. A., Spliet, W. G. M., Testerink, N., Berger, R., Ruiter, J. P. N., & van der Kolk, J. H. (2008). Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy. Neuromuscular Disorders, 18(5), 355-364. https://doi.org/10.1016/j.nmd.2008.02.007

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T1 - Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.

AU - Westermann, C.M.

AU - Dorland, L.

AU - Votion, D.M.

AU - de Sain - van der Velden, M.G.M.

AU - Wijnberg, I.D.

AU - Wanders, R.J.A.

AU - Spliet, W.G.M.

AU - Testerink, N.

AU - Berger, R.

AU - Ruiter, J.P.N.

AU - van der Kolk, J.H.

PY - 2008

Y1 - 2008

KW - Econometric and Statistical Methods: General

KW - Geneeskunde(GENK)

U2 - 10.1016/j.nmd.2008.02.007

DO - 10.1016/j.nmd.2008.02.007

M3 - Article

C2 - 18406615

SN - 0960-8966

VL - 18

SP - 355

EP - 364

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

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