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. 2022 Jul 1;9:913229. doi: 10.3389/fmed.2022.913229

FIGURE 1.

FIGURE 1

Genetic analysis indicated that the boy had a splicing variant (c.940-11G>A) of the OCRL gene. His mother carried a heterozygous mutation, whereas no mutation was detected in his father. Red arrow indicates the site of the mutant nucleotide.