HuGE Literature Finder
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 |
- Page last reviewed:Jul 25, 2022
- Page last updated:Jan 27, 2023
- Content source: