Germline Mutation in <i>KIF1Bβ</i> Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma

<div>Wild-type (a) and patient electropherogram showing the germline mutation p.Pro1351Leu in exon 38 of the <i>KIF1Bβ</i> gene (b) and the somatic mutation showing the LOH (c).</div>

International Journal of Endocrinology

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Figure 1: Germline Mutation in <i>KIF1Bβ</i> Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma 

Figure 1 | Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma 