Myotonic dystrophy type 1 (Steinert’s disease) is a multisystem disorder with autosomal dominant inheritance.

This disease is associated with the presence of an abnormal expansion of a cytosine thymine-guanine (CTG) trinucleotide repeat on chromosome 19q13.3. Because of rhythmic complications, the place for systematic electrophysiological study (EPS) has to be discussed.

Source: Biotechnology BioMed

Tags: Leo, Chromosome, Presence, Steiner, Technology

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