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. 2016 Feb 24;2016:bcr2015213939. doi: 10.1136/bcr-2015-213939

Figure 3.

Figure 3

DNA sequencing of the patient's HSD3B2 gene. Partial nucleotide sequence of the sense strand of axon 4 of the HSD3B2 gene, depicting a homozygous missense mutation. A nucleotide substitution is indicated by an arrow from the WT sequence CCA (Pro) to ACA (Thr)—P222T.