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. 2017 Apr 27;7:1219. doi: 10.1038/s41598-017-01182-9

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Sequencing results of nine novel disease-causing mutations. (A) Forward sequencing showed c.26C > T mutation of CRYBA4 gene in patients from family 1. (B) Reverse sequencing showed c.53G > A mutation of CRYGS gene in patients from family 4. (C) Forward sequencing showed p.G91del mutation of CRYBA1 gene in patients from family 5. (D) Forward sequencing showed c.224_225GC > TT mutation of CRYGS gene in patients from family 7. (E) Forward sequencing showed c.607C > T mutation CRYBA1 gene in patients from family 9. (F) Reverse sequencing showed c.452G > A of CRYBB2 gene in patientsfamily 17. (G) Reverse sequencing showed c.625 + 3A > G mutation of BFSP1gene in patients from family 19. (H) Forward sequencing showed c.795delA mutation of PAX6 gene in patient from family 24. (I) Forward sequencing showed c.342G > A mutation of PAX6gene in patients family 27.