A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of inherited metabolic disease 1996-01, Vol.19 (2), p.115-118
Hauptverfasser:	Seneca, S., Abramowicz, M., Lissens, W., Muller, M. F., Vamos, E., Meirleir, L.
Format:	Artikel
Sprache:	eng
Schlagworte:	Acidosis, Lactic - genetics Base Sequence Biological and medical sciences Cells, Cultured DNA, Mitochondrial - genetics Errors of metabolism Female Fibroblasts - chemistry Gene Deletion Humans Infant, Newborn Lymphocytes - chemistry Medical sciences Metabolic diseases Miscellaneous hereditary metabolic disorders Molecular Sequence Data Polymerase Chain Reaction Polymorphism, Single-Stranded Conformational
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