Fig. 3From: Multiple endocrine neoplasia type 1: a new germline “homozygous” variant (c.201delC) caused by detection errorsSanger sequencing results. The c.201delC change of NM_130802 in exon 2, which caused amino acid changes (p.Ala68Profs*51) that may have led to MEN1. The genetic changes were heterozygous variants (3rd times detection), but was wrongly detected as homozygous variants (1st, 2nd times detection)Back to article page