Molecular identification of missense variants in SLC3A1 gene; an approach leading to computer-aided drug design for cystinuria

Author:

Zafar RimshaORCID,Awais MuhammadORCID

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference43 articles.

1. PLIP 2021: expanding the scope of the protein–ligand interaction profiler to DNA and RNA;Adasme;Nucleic Acids Res.,2021

2. Predicting functional effect of human missense mutations using PolyPhen-2;Adzhubei;Curr. Protoc. Hum. Genet.,2013

3. How should patients with cystine stone disease be evaluated and treated in the twenty-first century?;Andreassen;Urolithiasis,2016

4. Clinical and molecular findings in a patient with a novel mutation in the deafness–dystonia peptide (DDP1) gene;Binder;Brain,2003

5. The PSIPRED protein analysis workbench: 20 years on;Buchan;Nucleic Acids Res.,2019

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