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GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
Eur Arch Otorhinolaryngol. 2015 Sep;272(9):2255-9. doi: 10.1007/s00405-014-3171-7. Epub 2014 Jul 11.
Eur Arch Otorhinolaryngol. 2015.
PMID: 25012701
In silico analysis of novel mutations in maple syrup urine disease patients from Iran.
Abiri M, Karamzadeh R, Mojbafan M, Alaei MR, Jodaki A, Safi M, Kianfar S, Bandehi Sarhaddi A, Noori-Daloii MR, Karimipoor M, Zeinali S.
Abiri M, et al.
Metab Brain Dis. 2017 Feb;32(1):105-113. doi: 10.1007/s11011-016-9867-1. Epub 2016 Aug 10.
Metab Brain Dis. 2017.
PMID: 27507644
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