Pearson marrow pancreas syndrome: a molecular study and clinical management - Seneca, Sara; Meirleir, Linda De; Scbepper, Jean De; Balduck, Nadine; Jochmans, Kristin; Liebaers, Inge; Lissens, Willy (Clinical genetics, 1997)
Keywords: Abnormalities, Multiple - drug therapy; Abnormalities, Multiple - genetics; Acidosis, Lactic - drug therapy; Acidosis, Lactic - genetics; Biological and medical sciences; Blotting, Southern; Bone Marrow Diseases - genetics; Bone Marrow Diseases - pathology; Child, Preschool; Complex syndromes; Diarrhea - drug therapy; Diarrhea - genetics; dichloroacetate (DCA); DNA, Mitochondrial; Failure to Thrive - genetics; Humans; Male; Medical genetics; Medical sciences; mt DNA deletions; Pancreatic Diseases - drug therapy; Pancreatic Diseases - genetics; Pearson syndrome; Restriction Mapping; Sequence Deletion; Syndrome; Human; Genetic inheritance; Pearson syndrome; Metabolic diseases; Male; Mitochondrial DNA; Enzymopathy; Congenital disease; Mitochondrial disorder; Case study; Deletion; Complex syndrome; Child