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A child with duchenne muscular dystrophy: A case report of a rare diagnosis among Africans - Nassoro - 2020 - Clinical Case Reports - Wiley Online Library
Deletion mutations in Duchenne muscular dystrophy (DMD) in Western Saudi children - ScienceDirect
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PDF) Analysis of Dystrophin Gene Deletions Indicates that the Hinge III Region of the Protein Correlates with Disease Severity
PDF) Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene
