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[Mitochondrial diseases]
J D Nagel1, F Haverkamp, M J Lentze
1Zentrum für Kinderheilkunde, Universität Bonn.
Klinische Padiatrie
|January 31, 1998
Summary
Mitochondrial diseases present diverse symptoms, making clinical diagnosis difficult. Simple biochemical tests offer a reliable and rapid method for identifying these complex genetic disorders.
Area of Science:
- Biochemistry
- Genetics
- Molecular Biology
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