Records 1 - 2
| Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss.
International journal of molecular and cellular medicine 2013 2 (1): 41-5.
Taghizadeh Seyyed Hossein, Kazeminezhad Seyyed Reza, Sefidgar Seyyed Ali Asghar, Yazdanpanahi Nasrin, Tabatabaeifar Mohammad Amin, Yousefi Ahmad, Lesani Seyyed Mohammad, Abolhasani Marziyeh, Hashemzadeh Chaleshtori Morte
| The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.
Molecular biology reports 2012 Dec 39 (12): 11011-6.
Charif Majida, Bounaceur Safaa, Abidi Omar, Nahili Halima, Rouba Hassan, Kandil Mostafa, Boulouiz Redouane, Barakat Abdelham