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What is the Ocular phenotype associated with a dystrophin deletion of exons 12-29?

Brignol TN, Ventura DF. What is the Ocular phenotype associated with a dystrophin deletion of exons 12-29? Intractable & rare diseases research 2018;7:295-296   Abstract Duchenne muscular dystrophy (DMD) is a result of a X-linked recessive inherited mutation of the DMD gene which contains 79 exons. This rare disease is passed on by the mother […]

World Duchenne
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