Identification of Novel Mutations in Spatacsin and Apolipoprotein B Genes in a Patient with Spastic Paraplegia and Hypobetalipoproteinemia
Sangers sequencing results of the APOB (NM_000384.2) variants identified by whole exome sequencing of the patient. (a) Showing the variant c.3337G > C in exon 22 and (b) showing the variant c.11333C > A in exon 26 of the APOB gene.
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