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Journal of Pediatric Neurosciences|January 12, 2022
Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with <i>MTHFR</i> Gene Mutation and Mitochondrial Complex I Deficiency: A Rare AssociationRohan R Mahale, Jyothi Gautam, Gautam Arunachal, et al.
Stem Cell Research|April 30, 2026
Generation of iPSC line NIMHi033-A from an Indian patient with Autism Spectrum Disorder carrying mutation in DYNC1H1 geneAshitha Siddappa Niranjana Murthy, Princy Choudhary, Pranshu Sachdeva, et al.
Science (New York, N.Y.)|October 14, 2021
Genomic characterization and epidemiology of an emerging SARS-CoV-2 variant in Delhi, IndiaMahesh S Dhar, Robin Marwal, Radhakrishnan Vs, et al.
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