Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Arash Hejazifar"'
Autor:
Naeimeh Tayebi, Oyediran Akinrinade, Muhammad Imran Khan, Arash Hejazifar, Alireza Dehghani, Frans P.M. Cremers, Mohammadreza Akhlaghi
Publikováno v:
Molecular Vision, Vol 25, Iss 1, Pp 106-117 (2019)
Purpose: Inherited retinal diseases (IRDs) are clinically and genetically heterogeneous showing progressive retinal cell death which results in vision loss. IRDs include a wide spectrum of disorders, such as retinitis pigmentosa (RP), Leber congenita
Externí odkaz:
https://doaj.org/article/68f3897dd08a42cdb4e2acc575916597
Autor:
Mojgan Rezaei, Majid Kheirollahi, Arash Hejazifar, Erfan Khorram, Maryam Riahinezhad, Omid Iravani, Mehdi Khorrami, Omid Yaghini, Vida Yazdani
Publikováno v:
Journal of molecular neuroscience : MNReferences. 71(11)
Vanishing white matter disease (VWM) is a rare autosomal recessive leukodystrophy caused by a mutation in any of the five gene encoding subunits of the translation initiation factors eIF2B1 to eIF2B5. Whole-exome sequencing was performed on a 7-year-
Autor:
Mohammad Amin Tabatabaiefar, Maryam Riahinezhad, Omid Yaghini, Erfan Khorram, Majid Kheirollahi, Mehdi Khorrami, Mojgan Rezaei, Arash Hejazifar
Publikováno v:
Journal of human genetics. 66(10)
In recent years, the tropomyosin-receptor kinase fused gene (TFG) has been linked to diverse hereditary neurodegenerative disorders, including a very rare complex hereditary spastic paraplegia, named spastic paraplegia type 57 (SPG57). Until now, fou