A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan
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* Corresponding author: Jamil Ahmad jamil_48@yahoo.co.in
BMC Medical Genetics 2008, 9:99 doi:10.1186/1471-2350-9-99
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 12 Jun 2008 | |
| Reviewer's Report | James Hejtmancik | 26 Jun 2008 | |
| Reviewer's Report | James Hejtmancik | 26 Jun 2008 | |
| Reviewer's Report | Colin Willoughby | 27 Jul 2008 | |
| Reviewer's Report | Chitra Kannabiran | 01 Aug 2008 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 17 Sep 2008 |
| Reviewer's Report | Colin Willoughby | 06 Oct 2008 | |
| Editorial acceptance | 06 Nov 2008 | ||
| Published | 11 Nov 2008 |