Salma Ben Salem

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1

M. Khairallah, P. Söderkvist, A. Rebaï, 2009, Human Genetics.

Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene.

L. Al-Gazali, B. Ali, J. Hertecant, 2012, European journal of medical genetics.

Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice

Richard S. Smith, P. Söderkvist, G. Howell, 2011, Nature Genetics.