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Journal Article

Kaushik, P and Mahajan, N and Girimaji, S C and Kumar, A (2020) Whole Exome Sequencing Identifies a Novel Homozygous Duplication Mutation in the VPS13B Gene in an Indian Family with Cohen Syndrome. In: Journal of Molecular Neuroscience, 70 (8). pp. 1225-1228.

This list was generated on Thu Mar 28 21:45:16 2024 IST.