|
|||||
|
|
Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome |
|
| Authors: | Alireza Haghighi Amit Tiwari Niloofar Piri Gudrun Nürnberg Nasrollah Saleh-Gohari Amirreza Haghighi John Neidhardt Peter Nürnberg Wolfgang Berger |
| Abstract: | |
| Keywords: | |