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...
Main Authors: | Ammara Akhtar, Sobia Nazir Ch, Mureed Hussain |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2021-01-01
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Series: | Informatics in Medicine Unlocked |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2352914821001003 |
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