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Fig. 4 | BMC Neurology

Fig. 4

From: Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review

Fig. 4

Sanger sequencing and cDNA analysis. a: Sanger sequencing of the PGAP1 gene in patient II-1 (upper row) and a control (lower row). The arrows indicated the compound heterozygous mutations. b: Agarose gel electrophoresis of cDNA from blood of Patient II-1 on the right and healthy control on the left. The red rectangles indicate the eluted bands using for subsequently sequencing. Letter a, b and c refer to the corresponding sequences on the right

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