Brain disease and molecular analysis in myotonic dystrophy

ABNORMAL amplification of a CTG repeat on chromosome 19 is the molecular basis of myotonic dystrophy (DM). Expansion of the repeat has been correlated with severity of several clinical features of the disease. We performed extensive cognitive testing, cerebral magnetic resonance imaging (MRI) and a...

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Veröffentlicht in:	Neuroreport 1994-12, Vol.5 (18), p.2549-2552
Hauptverfasser:	Damian, M S, Bachmann, G, Koch, M C, Schilling, G, Stoppler, S, Dorndorf, W
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Brain Diseases - diagnosis Brain Diseases - etiology Cognition Diseases of striated muscles. Neuromuscular diseases Female Humans Magnetic Resonance Imaging Male Medical sciences Middle Aged Myotonic Dystrophy - complications Myotonic Dystrophy - genetics Myotonic Dystrophy - psychology Neurology Psychometrics - methods Repetitive Sequences, Nucleic Acid
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