Running head: PERSPECTIVES ON ADHD

Mutations of the human plectin (Plec1) gene on chromosome 8q24 cause epidermolysis bullosa simplex with muscular dystrophy (EBS-MD). This rare autosomal recessive disorder is characterized by blistering of skin and mucous membranes since birth and progressive muscular dystrophy manifesting from infancy to the fourth decade of life. ................
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