Spinal Muscular Atrophy - Neurologic Clinics
Figure 5 from Spectrum of mutations in Duchenne Muscular Dystrophy (DMD) and clinical phenotype correlation in Sri Lankan population. | Semantic Scholar
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The identification of point mutations in Duchenne muscular dystrophy patients by using reverse-transcription PCR and the protein truncation test. - Abstract - Europe PMC
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
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Agriculture | June 2022 - Browse Articles
Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. - Abstract - Europe PMC
PDF) Analysis of Dystrophin Gene Deletions Indicates that the Hinge III Region of the Protein Correlates with Disease Severity
A child with duchenne muscular dystrophy: A case report of a rare diagnosis among Africans - Nassoro - 2020 - Clinical Case Reports - Wiley Online Library
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