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Genetic Diagnosis of Duchenne and Becker Muscular Dystrophy using Multiplex Ligation-Dependent Probe Amplification in Rwandan Patients

Odinaka KK, Nwolisa EC. Challenges in the management of the child with Duchenne muscular dystrophy in a resource poor setting:a case report. The Pan African medical journal 2014;19:227.   Abstract Duchenne muscular dystrophy is a progressive genetic disease with no cure at present. Children suffering from this disease eventually become wheelchair bound and die in […]