Identification of Novel Mutations in <i>Spatacsin</i> and <i>Apolipoprotein B</i> Genes in a Patient with Spastic Paraplegia and Hypobetalipoproteinemia

<div>Sangers sequencing results of the<i> APOB</i> (NM_000384.2) variants identified by whole exome sequencing of the patient. (a) Showing the variant c.3337G &gt; C in exon 22 and (b) showing the variant c.11333C &gt; A in exon 26 of the<i> APOB</i> gene.</div>

Case Reports in Genetics

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Figure 2: Identification of Novel Mutations in <i>Spatacsin</i> and <i>Apolipoprotein B</i> Genes in a Patient with Spastic Paraplegia and Hypobetalipoproteinemia 

Case Reports in Genetics

Identification of Novel Mutations in Spatacsin and Apolipoprotein B Genes in a Patient with Spastic Paraplegia and Hypobetalipoproteinemia

Figure 2