Manèl Chograni

The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly

Manèl Chograni, Imen Rejeb, Lamia Ben Jemâa et al. · European Journal of Human Genetics · 2011 · 22 citations · Full text

Autosomal recessive congenital cataract, intellectual disability phenotype linked to <i><scp>STX3</scp></i> in a consanguineous Tunisian family

Manèl Chograni, Fowzan S. Alkuraya, I. Ourteni et al. · Clinical Genetics · 2014 · 14 citations

RGS6: A Novel Gene Associated With Congenital Cataract, Mental Retardation, and Microcephaly in a Tunisian Family

Manèl Chograni, Fowzan S. Alkuraya, Faouzi Mâazoul et al. · Investigative Ophthalmology & Visual Science · 2014 · 13 citations