Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

R. J. Wanders; C. W. van Roermund; S. Brul; R. B. Schutgens; J. M. Tager

doi:10.1007/BF02435983

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

R. J. Wanders
, C. W. van Roermund
, S. Brul
, R. B. Schutgens
, J. M. Tager

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

Original language	English
Pages (from-to)	385-388
Journal	Journal of inherited metabolic disease
Volume	15
Issue number	3
DOIs	https://doi.org/10.1007/BF02435983
Publication status	Published - 1992

Access to Document

10.1007/BF02435983

Cite this

Wanders, R. J., van Roermund, C. W., Brul, S., Schutgens, R. B., & Tager, J. M. (1992). Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis. Journal of inherited metabolic disease, 15(3), 385-388. https://doi.org/10.1007/BF02435983

@article{2273f7a86b8b46958e979f490ea4a3ee,

title = "Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis",

author = "Wanders, \{R. J.\} and \{van Roermund\}, \{C. W.\} and S. Brul and Schutgens, \{R. B.\} and Tager, \{J. M.\}",

year = "1992",

doi = "10.1007/BF02435983",

language = "English",

volume = "15",

pages = "385--388",

journal = "Journal of inherited metabolic disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

number = "3",

}

Wanders, RJ , van Roermund, CW, Brul, S, Schutgens, RB & Tager, JM 1992, 'Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis', Journal of inherited metabolic disease, vol. 15, no. 3, pp. 385-388. https://doi.org/10.1007/BF02435983

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis. / Wanders, R. J.; van Roermund, C. W.; Brul, S. et al.
In: Journal of inherited metabolic disease, Vol. 15, No. 3, 1992, p. 385-388.

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

TY - JOUR

T1 - Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

AU - Wanders, R. J.

AU - van Roermund, C. W.

AU - Brul, S.

AU - Schutgens, R. B.

AU - Tager, J. M.

PY - 1992

Y1 - 1992

U2 - 10.1007/BF02435983

DO - 10.1007/BF02435983

M3 - Article

C2 - 1357231

SN - 0141-8955

VL - 15

SP - 385

EP - 388

JO - Journal of inherited metabolic disease

JF - Journal of inherited metabolic disease

IS - 3

ER -