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. 2024 Mar 4;15(3):333. doi: 10.3390/genes15030333

Figure 1.

Figure 1

A homozygous missense variant in HELQ. (A) IGV view of HELQ variant (c.596 A>C; p.(Gln199Pro)) variant in an isolated POI patient. (B) Sanger sequencing of the patient was consistent with the WES results. (C) Decipher view of the variant indicating conservation of the affected residue among the different species.