Impact of missense mutations in survival motor neuron protein (SMN1) leading to Spinal Muscular Atrophy (SMA): A computational approach
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology,Biochemistry
Link
http://link.springer.com/article/10.1007/s11011-018-0285-4/fulltext.html
Reference61 articles.
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3. Agrahari AK, Kumar A, Sneha P, Zayed H, George Priya Doss C (2018a) Substitution impact of highly conserved arginine residue at position 75 in GJB1 gene in association with X-linked Charcot-Marie-tooth disease: A computational study. J Theor Biol 437:305–317
4. Agrahari AK, Sneha P, George Priya Doss C, Siva R, Zayed H (2017) A profound computational study to prioritize the disease-causing mutations in PRPS1 gene. Metab Brain Dis. https://doi.org/10.1007/s11011-017-0121-2
5. Ali SK, Sneha P, Priyadharshini Christy J, Zayed H, George Priya Doss C (2017) Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation. J Biomol Struct Dyn 35(12):2714–2724
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