Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation

A. B. van Kuilenburg; P. Vreken; D. Riva; G. Botteon; N. G. Abeling; H. D. Bakker; A. H. van Gennip

doi:10.1023/A:1005470524203

Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation

A. B. van Kuilenburg
, P. Vreken
, D. Riva
, G. Botteon
, N. G. Abeling
, H. D. Bakker
, A. H. van Gennip

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

Original language	English
Pages (from-to)	191-192
Journal	Journal of inherited metabolic disease
Volume	22
Issue number	2
DOIs	https://doi.org/10.1023/A:1005470524203
Publication status	Published - 1999

Access to Document

10.1023/A:1005470524203

Cite this

@article{b819ace4fafc4247a0427b396cb518f6,

title = "Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation",

author = "\{van Kuilenburg\}, \{A. B.\} and P. Vreken and D. Riva and G. Botteon and Abeling, \{N. G.\} and Bakker, \{H. D.\} and \{van Gennip\}, \{A. H.\}",

year = "1999",

doi = "10.1023/A:1005470524203",

language = "English",

volume = "22",

pages = "191--192",

journal = "Journal of inherited metabolic disease",

issn = "0141-8955",

publisher = "Springer Netherlands",

number = "2",

}

TY - JOUR

T1 - Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation

AU - van Kuilenburg, A. B.

AU - Vreken, P.

AU - Riva, D.

AU - Botteon, G.

AU - Abeling, N. G.

AU - Bakker, H. D.

AU - van Gennip, A. H.

PY - 1999

Y1 - 1999

U2 - 10.1023/A:1005470524203

DO - 10.1023/A:1005470524203

M3 - Article

C2 - 10234617

SN - 0141-8955

VL - 22

SP - 191

EP - 192

JO - Journal of inherited metabolic disease

JF - Journal of inherited metabolic disease

IS - 2

ER -