Links
[1] http://ghr.nlm.nih.gov/gene/ACTG1
[2] https://disorders.eyes.arizona.edu/disorders/baraitser-winter-syndrome-2
[3] http://www.ncbi.nlm.nih.gov/omim/614583
[4] https://disorders.eyes.arizona.edu/disorders/temtamy-syndrome
[5] http://omim.org/entry/218340
[6] https://disorders.eyes.arizona.edu/references/exome-sequencing-identifies-compound-heterozygous-mutations-c12orf57-two-siblings-severe-
[7] https://disorders.eyes.arizona.edu/references/mutations-c12orf57-cause-syndromic-form-colobomatous-microphthalmia
[8] https://disorders.eyes.arizona.edu/references/previously-apparently-undescribed-syndrome-shallow-orbits-ptosis-coloboma-trigonocephaly
[9] https://disorders.eyes.arizona.edu/references/iris-coloboma-ptosis-hypertelorism-and-mental-retardation-new-syndrome