BMC Medical Genetics

official impact factor 2.44

Open Access Pre-publication history

A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan

Naheed Sajjad, Ingrid Goebel, Naseebullah Kakar, Abdul M Cheema, Christian Kubisch and Jamil Ahmad*

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