BMC Medical Genetics

official impact factor 2.44

Open Access Email this article to a friend

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

Fields marked * are required


Multiple email addresses should be separated with commas or semicolons.