X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts

R. J. Wanders; C. W. van Roermund; M. J. van Wijland; R. B. Schutgens; A. W. Schram; J. M. Tager; H. van den Bosch; C. Schalkwijk

doi:https://doi.org/10.1007/BF01804228

X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts

R. J. Wanders, C. W. van Roermund, M. J. van Wijland, R. B. Schutgens, A. W. Schram, J. M. Tager, H. van den Bosch, C. Schalkwijk

Other Departments

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

31 Citations (Scopus)

Original language	English
Pages (from-to)	173-177
Journal	Journal of Inherited Metabolic Disease
Volume	11
Issue number	Suppl. 2
DOIs	https://doi.org/10.1007/BF01804228
Publication status	Published - 1988

Access to Document

https://doi.org/10.1007/BF01804228

Cite this

Wanders, R. J., van Roermund, C. W., van Wijland, M. J., Schutgens, R. B., Schram, A. W., Tager, J. M., van den Bosch, H., & Schalkwijk, C. (1988). X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts. Journal of Inherited Metabolic Disease, 11(Suppl. 2), 173-177. https://doi.org/10.1007/BF01804228

Wanders, R. J. ; van Roermund, C. W. ; van Wijland, M. J. et al. / X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts. In: Journal of Inherited Metabolic Disease. 1988 ; Vol. 11, No. Suppl. 2. pp. 173-177.

@article{b3a409e4855f4bb7bf3467546fcc1190,

title = "X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts",

author = "Wanders, {R. J.} and {van Roermund}, {C. W.} and {van Wijland}, {M. J.} and Schutgens, {R. B.} and Schram, {A. W.} and Tager, {J. M.} and {van den Bosch}, H. and C. Schalkwijk",

year = "1988",

doi = "https://doi.org/10.1007/BF01804228",

language = "English",

volume = "11",

pages = "173--177",

journal = "Journal of Inherited Metabolic Disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

number = "Suppl. 2",

}

Wanders, RJ , van Roermund, CW, van Wijland, MJ, Schutgens, RB, Schram, AW, Tager, JM, van den Bosch, H & Schalkwijk, C 1988, 'X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts', Journal of Inherited Metabolic Disease, vol. 11, no. Suppl. 2, pp. 173-177. https://doi.org/10.1007/BF01804228

X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts. / Wanders, R. J.; van Roermund, C. W.; van Wijland, M. J. et al.
In: Journal of Inherited Metabolic Disease, Vol. 11, No. Suppl. 2, 1988, p. 173-177.

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

TY - JOUR

T1 - X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts

AU - Wanders, R. J.

AU - van Roermund, C. W.

AU - van Wijland, M. J.

AU - Schutgens, R. B.

AU - Schram, A. W.

AU - Tager, J. M.

AU - van den Bosch, H.

AU - Schalkwijk, C.

PY - 1988

Y1 - 1988

U2 - https://doi.org/10.1007/BF01804228

DO - https://doi.org/10.1007/BF01804228

M3 - Article

C2 - 3141702

SN - 0141-8955

VL - 11

SP - 173

EP - 177

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

IS - Suppl. 2

ER -

Wanders RJ , van Roermund CW, van Wijland MJ, Schutgens RB, Schram AW, Tager JM et al. X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts. Journal of Inherited Metabolic Disease. 1988;11(Suppl. 2):173-177. doi: https://doi.org/10.1007/BF01804228