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I. E. T. van den Berg
I. E. T. van den Berg
Biology
Point mutation
Mutation
Human liver
Genetics
2
Papers
60
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Tyrosinaemia type I—de novo mutation in liver tissue suppressing an inborn splicing defect
2005
Journal of Molecular Medicine
Y. T. Bliksrud
Else Brodtkorb
P. A. Andresen
I. E. T. van den Berg
Eli Anne Kvittingen
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Citations (26)
X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.
2004
American Journal of Human Genetics
I. E. T. van den Berg
E. A. C. M. van Beurden
Helga E.M. Malingré
H. K. Ploos van Amstel
Bwee-Tien Poll-The
Jan A M Smeitink
W.H. Lamers
Rudolphus Berger
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Citations (34)
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