Links
[1] http://ghr.nlm.nih.gov/gene/SIPA1L3#conditions
[2] https://disorders.eyes.arizona.edu/references/sipa1l3-identified-linkage-analysis-and-whole-exome-sequencing-novel-gene-autosomal
[3] https://disorders.eyes.arizona.edu/references/mutations-sipa1l3-cause-eye-defects-through-disruption-cell-polarity-and-cytoskeleton