Molecular Investigation of Leber's Hereditary Optic Neuropathy Common Mutations in Suspected Patients
LHON is a mitochondrial neurodegenerative disorder often manifesting itself in the second or third decade of life, and hence resulting in progressive central vision loss usually in a short period of 2-8 weeks within which different degrees of blindness may occur. Etiologically, more than twenty miss...
Saved in:
Main Authors: | HR Soleimanpour (Author), DD Farhud (Author), SK Bidooki (Author), L Andonian (Author), M Togha (Author), M Khanlari (Author) |
---|---|
Format: | Book |
Published: |
Tehran University of Medical Sciences,
2004-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Molecular Investigation of Leber's Hereditary Optic Neuropathy Common Mutations in Suspected Patients
by: HR Soleimanpour, et al.
Published: (2004) -
Antiretroviral therapy-induced Leber's hereditary optic neuropathy
by: Anand Moodley, et al.
Published: (2014) -
Leber Hereditary Optic Neuropathy: Do Folate Pathway Gene Alterations Influence the Expression of Mitochondrial DNA Mutation?
by: A Aleyasin, et al.
Published: (2010) -
Leber Hereditary Optic Neuropathy: Do Folate Pathway Gene Alterations Influence the Expression of Mitochondrial DNA Mutation?
by: A Aleyasin, et al.
Published: (2010) -
Atypical Leber's Optic Neuropathy
by: J Gordon Millichap
Published: (1993)