Publications by authors named "Eveline Jongen"

2Publications

Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.

Authors:
Mike Gerards Rick Kamps Jo van Oevelen Iris Boesten Eveline Jongen Bart de Koning Hans R Scholte Isabel de Angst Kees Schoonderwoerd Abdelaziz Sefiani Ilham Ratbi Wouter Coppieters Latifa Karim René de Coo Bianca van den Bosch Hubert Smeets

Brain 2013 Mar 18;136(Pt 3):882-90. Epub 2013 Feb 18.

Department of Genetics and Cell Biology, P.O. Box 616, 6200 MD Maastricht, the Netherlands.

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March 2013

Mitochondrial DNA damage analysis in bronchoalveolar lavage cells of preterm infants.

Authors:
Bea Zoer Jasper Valentijn Been Eveline Jongen Anne Debeer Alexandra Hendrickx Hubertus J Smeets Luc Jacques Zimmermann Eduardo Villamor

Front Biosci (Elite Ed) 2010 Jan 1;2:361-8. Epub 2010 Jan 1.

Department of Pediatrics Maastricht University Medical Center, GROW School for Oncology and Developmental Biology, 6202 AZ Maastricht, The Netherlands.

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January 2010