In silico computation of functional SNPs of CYP2U1 protein leading to hereditary spastic paraplegia

In silico computation of functional SNPs of CYP2U1 protein leading to hereditary spastic paraplegia

Hereditary spastic paraplegia is a genetically heterogeneous neurological disease mainly characterized by growing spasticity in a lower limb area. Spastic paraplegia 56 (SPG56) causes the autosomal recessive form of hereditary spastic paraplegia. Over time, many attempts have been made to find heter...

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Bibliographic Details
Main Authors: Ammara Akhtar, Sobia Nazir Ch, Mureed Hussain
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Informatics in Medicine Unlocked
Subjects:
Hereditary spastic paraplegia
CYP2U1
SPG56
Missense
Variants
SNPs
Online Access:http://www.sciencedirect.com/science/article/pii/S2352914821001003

Internet

http://www.sciencedirect.com/science/article/pii/S2352914821001003

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