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A Novel Retinal Identification System

โœ Scribed by Farzin, Hadi ;Abrishami-Moghaddam, Hamid ;Moin, Mohammad-Shahram

Book ID
120382438
Publisher
Hindawi Limited
Year
2008
Tongue
English
Weight
318 KB
Volume
2008
Category
Article
ISSN
1110-8657

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Retinitis pigmentosa (RP) is a group of genetically heterogeneous retinal degenerations that can be autosomal dominant (ADRP), autosomal recessive (ARRP), or X-linked. Approximately 30% of ADRP patients show point mutations or small deletions in the rhodopsin gene. However, over 50% of the RP patien