Ghent University Academic Bibliography

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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

François-Guillaume Debray, Claudia Stümpfig, Arnaud Vanlander (UGent) , Vinciane Dideberg, Claire Josse, Jean-Hubert Caberg, François Boemer, Vincent Bours, René Stevens, Sara Seneca, et al.

(2015) JOURNAL OF INHERITED METABOLIC DISEASE. 38(6). p.1147-1153
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A homozygous mutation in IBA57 involved in intramitochondrial iron-sulfur cluster synthesis causes severe encephalopathy and mypathy in two neonates

Arnaud Vanlander (UGent) , Claudia Willbrecht, Nikhita Ajit Bolar, Joél Smet (UGent) , Boel De Paepe (UGent) , Elien De Latter (UGent) , Lut Van Laer (UGent) , Bart Loeys (UGent) , Roland Lill and Rudy Van Coster (UGent)

(2013) EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 17(suppl. 1). p.S5-S6
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy

Nikhita Ajit Bolar, Arnaud Vanlander (UGent) , Claudia Wilbrecht, Nathalie Van der Aa, Joél Smet (UGent) , Boel De Paepe (UGent) , Geert Vandeweyer, Frank Kooy, François Eyskens, Elien De Latter (UGent) , et al.

(2013) HUMAN MOLECULAR GENETICS. 22(13). p.2590-2602
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- Conference Paper
- C3
Mutation of the iron-sulfur cluster assembly IBA57 gene causes lethal myopathy and encephalopathy

N Ajit Bolar, Arnaud Vanlander (UGent) , C Wilbrecht, Nathalie Van der Aa, Joél Smet (UGent) , Boel De Paepe (UGent) , G Vandeweyer, F Kooy, François Eyskens, Elien De Latter (UGent) , et al.

(2013) EUROPEAN JOURNAL OF HUMAN GENETICS. 21(suppl. 2). p.30-30
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A mutation of the mitochondrial ABC transporter Sta1 leads to dwarfism and chlorosis in the Arabidopsis mutant starik

Sergei Kushnir (UGent) , Elena Babiychuk (UGent) , Serguei Storojenko (UGent) , Mark W Davey (UGent) , Jutta Papenbrock, Riet De Rycke (UGent) , Gilbert Engler (UGent) , Udo W Stephan, Heike Lange, Gyula Kispal, et al.

(2001) PLANT CELL. 13(1). p.89-100

Academic Bibliography

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

A homozygous mutation in IBA57 involved in intramitochondrial iron-sulfur cluster synthesis causes severe encephalopathy and mypathy in two neonates

Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy

Mutation of the iron-sulfur cluster assembly IBA57 gene causes lethal myopathy and encephalopathy

A mutation of the mitochondrial ABC transporter Sta1 leads to dwarfism and chlorosis in the Arabidopsis mutant starik

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