Large Region of Homozygous (ROH) Identified in Indian Patients with Autosomal Recessive Limb-Girdle Muscular Dystrophy with p.Thr182Pro Variant in <i>SGCB</i> Gene

<div>Ancestry analysis. (a) PCA value distribution of our study cases and controls overlaid with Genome Asia study. Our cases and control samples overlap South Asian ancestry data. (b) Proportion of South Asian (SAS) and West Eurasian (WES) predicted for case and control samples using admixture analysis. 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Human Mutation

fig2

Figure 2

Figure 2: Large Region of Homozygous (ROH) Identified in Indian Patients with Autosomal Recessive Limb-Girdle Muscular Dystrophy with p.Thr182Pro Variant in <i>SGCB</i> Gene 

Figure 2 | Large Region of Homozygous (ROH) Identified in Indian Patients with Autosomal Recessive Limb-Girdle Muscular Dystrophy with p.Thr182Pro Variant in SGCB Gene 