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Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency
M. C. Y. de Wit
, I. F. M. de Coo
, E. Verbeek
, R. Schot
, G. C. Schoonderwoerd
, M. Duran
, J. B. C. de Klerk
, J. G. M. Huijmans
, M. H. Lequin
, F. W. Verheijen
, G. M. S. Mancini
Affiliatie UvA
Research output
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Dive into the research topics of 'Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency'. Together they form a unique fingerprint.
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Medicine and Dentistry
Malonyl Coenzyme A Decarboxylase
100%
Brain Abnormalities
100%
Magnetic Resonance Imaging of Brain
50%
Cortical Dysplasia
50%
Myocardial Disease
25%
Physical Disease by Body Function
25%
Hypoglycemia
25%
Brain Development
25%
Transcription Regulation
25%
Macrogyria
25%
Inborn Error of Metabolism
25%
Malonyl-CoA
25%
Metabolic Acidosis
25%
Periventricular Heterotopia
25%
Keyphrases
Malonyl-CoA Decarboxylase Deficiency
100%
Brain Abnormalities
100%
Inborn Errors of Metabolism
25%
Malonyl-CoA
25%
Gene Sequence Analysis
25%
MLYCD
25%
Incomplete Understanding
25%
Neurological Signs
25%
Messenger
25%
Periventricular Nodular Heterotopia
25%
Biochemistry, Genetics and Molecular Biology
Malonyl-CoA Decarboxylase
100%
Magnetic Resonance Imaging
50%
Metabolic Pathway
25%
Brain Development
25%
Transcription Regulation
25%
Inborn Error of Metabolism
25%
Malonyl-CoA
25%
Immunology and Microbiology
Magnetic Resonance Imaging
100%
White Matter
50%
Brain Development
50%
Transcription Regulation
50%