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Whole Exome Sequencing Identifies a Novel Homozygous Duplication Mutation in the VPS13B Gene in an Indian Family with Cohen Syndrome
Kaushik, Pankhuri, Mahajan, Naresh, Girimaji, Satish C., Kumar, ArunLanguage:
english
Journal:
Journal of Molecular Neuroscience
DOI:
10.1007/s12031-020-01530-x
Date:
March, 2020
File:
PDF, 954 KB
english, 2020