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Figure 1 | BMC Research Notes

Figure 1

From: Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Figure 1

The pedigree of the family, and mutations identified in each member of the family, and respective eletroferogram of part of exon 102 and exon 98 of the RYR1 gene illustrating the missense alterations. Histological reactions showing HE, ATPase 4.3 and NADH staining, and immunohistochemical analysis for dystrophin, γ-SG and telethonin. (Magnification – X200).

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